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Syndactyly Type 7

Dr. Samantha A. Vergano, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist. Dr. Samantha A. Vergano, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist.
12 Views
Degenerative Bones, Joints, and Spine Care (A - Z)
  • Other names
  • Types of syndactyly type 7
  • Causes and risk factors
  • Symptoms and signs
  • Diagnostic tests
  • Non-pharmacological treatments (therapies others)
  • Drug treatments
  • Dietary molecular supplements
  • Drugs for immunity booster / regenerative / stem cell
  • Surgeries (procedures and why they are done)
  • Preventions
  • When to see a doctor
  • What to eat and what to avoid
  • FAQs

Syndactyly type 7 is a rare birth condition where some fingers (and sometimes toes) are joined together, often in a complex way (skin + soft tissue + sometimes bone). Many people also have changes in the forearm bones (for example, bones that are shaped differently or joined), so the hand may look “merged” and may not open or grip normally. It is usually linked to changes (variants) in a gene called LRP4 and is often autosomal recessive, meaning a child may be affected when they inherit a changed copy from both parents. Orpha.net+2Genetic Diseases Info Center+2

This condition is not caused by anything the child did, and most of the time it is not preventable after conception. Care focuses on: (1) understanding the exact bone/soft-tissue pattern, (2) protecting function, (3) planning surgery when helpful, and (4) long-term therapy and follow-up. PMC+2assh.org+2

Syndactyly type 7 is a rare condition present from birth where the fingers and/or toes do not separate normally, so they stay joined together. In this type, the joining is often complex, meaning not only the skin is joined, but some bones may also be fused or shaped in an unusual way. NCBI+2PMC+2

This condition can make the hand look like one “block” of digits because the normal finger bones may be hard to tell apart on an X-ray. The bones of the wrist and palm can also be mixed up or fused, so finger movement and hand function can be limited. NCBI+1

Syndactyly type 7 is most often caused by having two changed copies (one from each parent) of a gene called LRP4, so it usually follows an autosomal recessive inheritance pattern. Some people with this condition can also have kidney problems, so doctors often check the kidneys too. NCBI+2Cell+2

Other names

Syndactyly type 7 is also known by these names, and doctors may use any of them in reports: NCBI+2NCBI+2

  • Cenani–Lenz syndactyly syndrome (CLSS) NCBI

  • Cenani–Lenz syndrome (CLS) Orpha.net+1

  • Cenani syndactylism / Cenani syndactyly NCBI

Types of syndactyly type 7

Doctors have described two main “looks” (phenotypes) of syndactyly type 7. Here is the list view: PMC

  • Spoon-hand type (classic type) PMC

  • Oligodactyly type (variant type) PMC

Spoon-hand type (classic). In this type, many or all fingers are joined, and the hand can look broad and “spoon-shaped.” The finger bones and wrist bones may be fused or arranged in a confusing way, which can reduce normal bending and grasping. PMC+1

Oligodactyly type (variant). “Oligodactyly” means fewer digits than usual. In this type, there may be fewer fingers (or toes), and some finger bones may be missing, very short, or fused into one structure. This can strongly affect grip and fine hand use. PMC+1

Causes and risk factors

Important note: The direct cause of syndactyly type 7 is genetic (LRP4-related). The other items below are general causes or risk factors for syndactyly/digit-fusion in babies, and they can sometimes create “similar-looking” findings, but they are not the main cause of true syndactyly type 7. NCBI+2SpringerLink+2

1. Two disease-causing changes in the LRP4 gene (biallelic variants). This is the best-known direct cause of syndactyly type 7 and can disturb important limb-development signals during early growth of the baby. Cell+1

2. Autosomal recessive inheritance (both parents are carriers). Parents often have no symptoms, but each parent can carry one changed copy of the gene, and the child gets both copies. NCBI+1

3. Consanguinity (parents are blood relatives). When parents are related, there is a higher chance they carry the same rare gene change, which can raise the chance of recessive disorders like this one. PubMed+1

4. Disruption of normal “interdigital cell death.” Normally, the tissue between forming fingers/toes is removed by a controlled process, so digits separate; problems in these pathways can lead to joined digits. SpringerLink

5. Disturbance of WNT–BMP–FGF signaling balance. These signaling systems help guide digit growth and separation; changes can reduce separation signals and increase joining. SpringerLink+1

6. Other gene changes linked to syndactyly (not SD7 specific). Many syndactyly types are caused by different genes, so a baby can have syndactyly from another genetic condition that is not SD7. SpringerLink+1

7. New (de novo) genetic changes in limb genes (general). Sometimes a gene change starts in the baby for the first time; this is a known idea in many genetic limb conditions, even though SD7 is usually recessive. SpringerLink+1

8. Maternal cigarette smoking during pregnancy (risk for digit anomalies). Research has reported an association between smoking in pregnancy and higher risk of congenital digit differences, including webbed digits. PubMed+1

9. Poor nutrition in early pregnancy (general risk factor). Some studies and reviews note that lower nutritional status in early pregnancy can be linked with higher risk of congenital limb differences. SpringerLink+1

10. Low socioeconomic status (general association). Some research connects lower economic status with higher risk of some congenital anomalies, including digit differences, though this does not prove direct cause. SpringerLink+1

11. Pre-gestational diabetes (before pregnancy). Large studies show that diabetes before pregnancy is linked to increased risk of many congenital anomalies overall (birth differences), so careful pregnancy care matters. PLOS+1

12. Gestational diabetes (during pregnancy). Gestational diabetes has also been linked to a smaller but still measurable increase in risk for congenital anomalies overall in some large datasets. PLOS

13. Some anti-seizure medicines (general teratogenic concern). Certain anti-seizure drugs are known to raise birth-defect risks in general, and limb differences are part of the wider concern in teratology research. ResearchGate+1

14. Thalidomide exposure (historical teratogen). Thalidomide is a well-known cause of severe limb defects when taken in pregnancy, showing how sensitive limb development is early in pregnancy. PMC+1

15. Warfarin exposure (general teratogenic concern). Warfarin is a recognized teratogen, and teratology reviews list it among agents that can cause congenital defects, including limb problems. ResearchGate+1

16. Valproate exposure (general teratogenic concern). Valproate is widely discussed in pregnancy risk literature as teratogenic; limb defects are included within the broader set of possible congenital outcomes. ResearchGate+1

17. Misoprostol exposure (general teratogenic concern). Teratology reviews include misoprostol among exposures linked with limb defects in babies when taken during pregnancy. ResearchGate

18. Phenytoin exposure (general teratogenic concern). Phenytoin is also listed in teratology sources among drugs associated with congenital defect risks, including limb differences. ResearchGate+1

19. Exposure to hazardous substances before pregnancy (general). Some case-control research suggests that certain hazardous exposures before pregnancy may be associated with higher risk of digit anomalies. PubMed

20. Multifactorial causes (genes + environment together). Many congenital conditions happen from a mix of genetic tendency and environmental factors; reviews of syndactyly discuss both genetic pathways and outside influences. SpringerLink+1

Symptoms and signs

1. Joined fingers (hand syndactyly). Fingers may be joined by skin and also by bone, and the joining can involve many fingers at once. NCBI+1

2. Joined toes (foot syndactyly). Toes can also be joined, and the pattern can differ between people even in the same family. NCBI+1

3. Bone fusion in the fingers (phalangeal synostosis). X-rays may show finger bones fused together, which limits normal bending. NCBI+1

4. Bone fusion in the palm (metacarpal fusion). The long bones in the palm can be fused or disorganized, changing hand shape and function. NCBI+1

5. Disorganized wrist bones (carpal changes). Wrist bones can look irregular, fused, or not arranged in the usual pattern on imaging. PMC+1

6. “Spoon-hand” appearance (classic type). The hand may look broad and scoop-like because fingers are merged and bones are rearranged. PMC+1

7. Fewer fingers (oligodactyly type). Some people have fewer fingers than usual, which can strongly affect grip and fine movement. PMC+1

8. Short forearm bones (radius/ulna shortening). The radius and ulna can be shorter than usual, which may shorten the arm and limit movement. NCBI+1

9. Radioulnar synostosis (radius fused to ulna). The radius and ulna may be fused, making it hard to rotate the forearm (turning palm up/down). NCBI+1

10. Limited finger motion or stiff joints. Because bones and soft tissues are joined, fingers may not bend normally, and hand motion can be restricted. PMC+1

11. Reduced grip strength or hand function. Daily tasks like holding a pen or buttoning clothes can be hard, depending on how many fingers are involved. PMC+1

12. Mild facial differences (mild facial dysmorphism). Some people have mild facial features that look a bit different, but these can be subtle. NCBI+1

13. Dental (teeth) differences. Some reports and reviews mention tooth abnormalities as part of the wider syndrome picture in some patients. PMC+1

14. Kidney anomalies (renal agenesis/hypoplasia). Some people have missing kidneys or small kidneys, so kidney checks are important even if there are no symptoms at first. PubMed+1

15. Differences in walking or shoe-wear comfort (when feet are involved). Joined toes, short toes, or bone fusion can change balance or comfort, especially with tight shoes. NCBI+1

Diagnostic tests

Below are common tests doctors use to understand syndactyly type 7, check severity, and look for related issues like kidney differences. NCBI+2SpringerLink+2

Physical exam tests:

1. Hand and finger inspection. The doctor checks which fingers are joined, how far the joining goes, and whether nails and skin are separate or shared. SpringerLink+1

2. Foot and toe inspection. The doctor checks toes the same way, because toe joining is also common in this condition. NCBI

3. Range of motion exam. The doctor gently moves finger joints and wrist joints to see how much bending and straightening is possible. PMC+1

4. Neurovascular exam of the digits. The doctor checks warmth, color, capillary refill, and feeling to make sure blood flow and nerve function are okay. SpringerLink

5. Full dysmorphology exam (whole-body check). Because SD7 can be part of a wider syndrome, the doctor looks at face, teeth, limbs, and growth patterns. NCBI+1

Manual / functional tests:

6. Grip strength testing. Simple grip tests show how strongly the hand can hold, which helps plan therapy or surgery. PMC+1

7. Pinch strength testing. Pinch tests measure thumb-to-finger function, which is important for writing and small tasks. PMC

8. Dexterity testing (fine-motor tasks). Tasks like picking up small objects help show how the hand works in real life. PMC+1

9. Goniometry (angle measurement of joints). A small tool can measure joint angles to document stiffness and track change over time. SpringerLink

Lab and pathological / genetic tests:

10. LRP4 gene sequencing. A genetic test can look for disease-causing changes in LRP4, which is the key known gene for this syndrome. NCBI+1

11. Deletion/duplication testing of LRP4 (if sequencing is negative). Sometimes labs also check for missing or extra gene pieces that sequencing may miss. NCBI

12. Chromosomal microarray (when the diagnosis is unclear). This checks for large chromosome changes that can be linked to congenital differences, especially when many body systems are involved. SpringerLink

13. Carrier testing for parents (family planning). Parents can be tested to see if they carry the LRP4 variant found in the child, which helps explain inheritance. NCBI+1

14. Prenatal diagnostic testing (CVS or amniocentesis) when a family variant is known. If a family already knows the exact LRP4 change, prenatal genetic testing can sometimes check for that variant in a future pregnancy. NCBI+1

Electrodiagnostic tests (used when needed):

15. Nerve conduction study (NCS). If there are signs of nerve problems (numbness, weakness), doctors can test how well nerves carry signals. SpringerLink

16. Electromyography (EMG). EMG can be used if muscle weakness is suspected, to see how muscles and nerves work together. SpringerLink

Imaging tests:

17. X-ray of the hands. This is a key test to see bone fusion, missing bones, and the overall bone pattern of the hand. SpringerLink+1

18. X-ray of the feet. Foot X-rays show toe fusion and help explain walking or shoe problems. SpringerLink

19. Forearm X-ray (radius/ulna). This checks for radioulnar synostosis and shortening of the forearm bones. NCBI+1

20. Kidney ultrasound. Because kidney anomalies can happen in many patients, ultrasound is a safe way to look for missing or small kidneys. NCBI+1


Non-pharmacological treatments (therapies others)

1) Hand surgeon evaluation (congenital hand specialist). A specialist checks which fingers are fused, whether bones are shared, and how blood vessels and nerves run. The purpose is to choose the safest plan (observe vs surgery) and set realistic goals. Mechanism: careful exam + imaging review guides timing and technique. assh.org+1

2) Team care (orthopedics + plastics + OT). Syndactyly type 7 can involve hand, forearm, and function. Purpose: coordinate surgery, therapy, and growth monitoring. Mechanism: each expert handles one part (bones, skin coverage, movement training), reducing complications and improving use. PMC+1

3) Detailed functional assessment (grip, pinch, daily tasks). Testing how the hand works helps decide whether surgery is needed now or later. Purpose: match treatment to real-life needs (writing, dressing, eating). Mechanism: function scoring identifies the biggest limits and tracks progress over time. assh.org+1

4) Occupational therapy (OT) for hand skills. OT teaches simple, repeated practice for grasp, release, and fine motor control. Purpose: improve independence even before surgery. Mechanism: brain and muscle “retraining” improves coordination and strength through guided tasks. PMC+1

5) Hand stretching and range-of-motion routine. Gentle stretching keeps nearby joints from becoming stiff. Purpose: protect motion while the child grows and after procedures. Mechanism: slow, regular movement helps soft tissues stay flexible and reduces tightness. PMC

6) Splinting (custom night splints). Some patients benefit from splints to hold fingers in safer positions. Purpose: reduce joint bending deformities and help alignment. Mechanism: steady low force over hours can guide soft tissues and joint posture. PMC+1

7) Scar care education (after surgery). Families learn to keep scars soft and flat. Purpose: reduce thick scars and web “creep.” Mechanism: massage, silicone, and protection can reduce irritation and help scar remodeling. Washington University Orthopedics+1

8) Sensory play therapy. Joined fingers and surgeries can change sensation. Purpose: reduce “over-sensitive” or “under-sensitive” feelings and improve hand use. Mechanism: graded textures and safe touch training help the nervous system adapt. PMC

9) Adaptive tools for school and home. Pencil grips, modified scissors, and button hooks reduce frustration. Purpose: keep the child active and confident. Mechanism: tools “replace” missing pinch patterns so tasks become possible without pain. assh.org

10) Protective gloves for high-risk activities. Some hands are more easily injured because fingers cannot separate. Purpose: lower cuts/burns and reduce infection risk. Mechanism: a physical barrier prevents skin damage during sports, cooking, or crafts. assh.org

11) Physical therapy for forearm motion (if forearm bones involved). Some people have limited rotation or elbow/wrist motion. Purpose: maximize safe movement and strength. Mechanism: targeted exercises strengthen supporting muscles and train safe patterns. Genetic Diseases Info Center+1

12) Imaging-guided planning conference. Surgeons often review X-rays/CT with the team. Purpose: avoid harming blood supply and plan bone cuts if needed. Mechanism: mapping anatomy reduces unexpected findings in surgery. PMC+1

13) Staged treatment plan (more than one operation if needed). Complex syndactyly may require more than one stage. Purpose: protect finger blood flow and reduce risk. Mechanism: operating on one web space at a time prevents damage to both sides of a finger. GOSH Hospital site

14) Timing strategy for surgery. Many teams aim around the toddler years, but timing depends on which digits are involved. Purpose: support growth and function. Mechanism: earlier release may prevent growth pulling and deformity, especially when border digits are fused. PMC+1

15) Wound care training (after procedures). Families learn cleaning, dressing changes, and warning signs. Purpose: prevent infection and protect grafts/flaps. Mechanism: clean, moist-balanced wound care supports healing and reduces bacteria. GOSH Hospital site+1

16) Psychosocial support (confidence + bullying prevention). Visible hand differences can affect mood and school life. Purpose: build coping skills and self-advocacy. Mechanism: counseling and peer support improve resilience and social comfort. assh.org

17) Genetic counseling for the family. Because type 7 is often inherited, counseling explains risks for future pregnancies. Purpose: informed planning and options. Mechanism: reviewing inheritance patterns and testing helps families understand recurrence risk. NCBI+1

18) Prenatal and early-life planning (if diagnosed early). If suspected before birth, families can plan specialist visits after delivery. Purpose: reduce delays in care. Mechanism: early referral improves timely imaging, therapy, and surgical discussions. Orpha.net+1

19) Long-term follow-up through growth. As hands grow, scars can tighten and webs can creep. Purpose: catch problems early. Mechanism: regular checks allow quick therapy changes or revision planning if needed. Washington University Orthopedics+1

20) Lifestyle for healing (sleep + protein + activity). Strong healing needs good sleep and nutrition. Purpose: support recovery after procedures and therapy gains. Mechanism: sleep hormones and adequate nutrients help tissue repair and learning of new skills. Office of Dietary Supplements+1


Drug treatments

Important reality: Syndactyly type 7 is a structural (anatomy) condition, so medicines do not “unfuse” fingers. Drugs are mainly used for pain control, anesthesia, infection prevention/treatment, allergy control, and nausea around procedures. PMC+1

1) Acetaminophen (Tylenol) – pain/fever reducer. Used for mild to moderate pain after procedures. Class: analgesic/antipyretic. Dose/time: label includes adult dosing schedules (example ER products and limits); clinician sets pediatric dosing. Purpose: comfort and fever control. Mechanism: changes pain signaling in the brain. Side effects: liver injury risk with overdose or combining products. FDA Access Data+1

2) Ibuprofen – NSAID for pain/swelling. Often used after surgery if allowed. Class: NSAID. Dose/time: label has adult/12+ directions; clinician decides for children. Purpose: reduce pain and inflammation. Mechanism: blocks COX enzymes → fewer prostaglandins. Side effects: stomach bleeding risk, kidney stress, allergic reactions in some people. FDA Access Data+1

3) Naproxen sodium – longer-acting NSAID. Sometimes chosen for longer pain control in older teens/adults. Class: NSAID. Dose/time: label gives OTC directions and warnings. Purpose: pain and inflammation reduction. Mechanism: COX inhibition. Side effects: stomach bleeding, heart risk warnings, kidney effects; avoid mixing with other NSAIDs unless clinician says. FDA Access Data+1

4) Celecoxib (Celebrex) – selective NSAID (COX-2). May be used in some patients to reduce inflammation with different stomach-risk profile than some NSAIDs (still has serious warnings). Class: COX-2 selective NSAID. Dose/time: label-based dosing by clinician. Purpose: pain/inflammation control. Mechanism: COX-2 inhibition. Side effects: cardiovascular risk, GI risk still possible, kidney effects. FDA Access Data+1

5) Ketorolac (Toradol) – short-term strong NSAID. Sometimes used for short periods after surgery for severe pain, often in a hospital setting. Class: NSAID. Dose/time: labeling stresses short-term use and limits. Purpose: opioid-sparing pain control. Mechanism: COX inhibition. Side effects: bleeding, kidney injury, stomach ulcers—risk is why duration is limited. FDA Access Data+1

6) Tramadol – prescription pain medicine (opioid-like). Sometimes used for moderate pain when other options fail, but requires caution. Class: opioid agonist + monoamine reuptake effects. Dose/time: clinician follows labeling and age rules. Purpose: pain relief. Mechanism: opioid receptor activity + neurotransmitter effects. Side effects: sleepiness, nausea, dependence risk, and serious warnings including breathing risk. FDA Access Data+1

7) Oxycodone – opioid pain medicine. Used only when pain is severe and other treatments are not enough. Class: opioid analgesic. Dose/time: clinician uses label guidance; not for casual use. Purpose: strong pain relief. Mechanism: opioid receptor activation changes pain perception. Side effects: constipation, nausea, dependence, and dangerous breathing suppression (major warning). FDA Access Data+1

8) Hydrocodone + acetaminophen (e.g., Norco/Vicodin) – combination pain medicine. Sometimes used short-term after surgery. Class: opioid + non-opioid analgesic. Dose/time: label-based, clinician-set; must count total acetaminophen from all products. Purpose: pain control. Mechanism: opioid receptor effects + acetaminophen central pain control. Side effects: drowsiness, constipation, dependence, liver risk if acetaminophen limit exceeded. FDA Access Data+1

9) Morphine – opioid for severe pain (often hospital). Used in controlled settings for severe post-op pain. Class: opioid agonist. Dose/time: clinicians use labeling and monitor closely. Purpose: strong pain control. Mechanism: opioid receptor activation. Side effects: respiratory depression risk, low blood pressure, nausea, constipation; careful monitoring is standard. FDA Access Data+1

10) Lidocaine injection (Xylocaine) – local anesthetic. Used to numb tissue for procedures or nerve blocks (by clinicians). Class: local anesthetic (amide). Dose/time: clinician-calculated per label. Purpose: pain control during/after procedures. Mechanism: blocks sodium channels → stops nerve pain signals. Side effects: heart rhythm or CNS toxicity if too much enters bloodstream. FDA Access Data+1

11) Bupivacaine injection (Marcaine) – longer local anesthetic. Often used for longer numbness after surgery. Class: local anesthetic (amide). Dose/time: clinician-set. Purpose: longer pain relief around the surgical area. Mechanism: sodium channel blockade. Side effects: serious heart toxicity risk with overdose—handled by trained anesthesia teams. FDA Access Data+1

12) Ondansetron (Zofran) – anti-nausea medicine. Common after anesthesia or opioids. Class: 5-HT3 receptor antagonist. Dose/time: clinician per label and age. Purpose: prevent/treat nausea and vomiting. Mechanism: blocks serotonin signaling that triggers vomiting. Side effects: headache, constipation; QT-related heart rhythm risk in some patients. FDA Access Data+1

13) Diphenhydramine – antihistamine for itching/allergy. Sometimes used for itching from opioids or mild allergic reactions (clinician guidance). Class: H1 antihistamine. Dose/time: label-based. Purpose: relieve itching, hives, allergy symptoms. Mechanism: blocks histamine H1 receptors. Side effects: sleepiness, dry mouth; can impair attention and coordination. FDA Access Data

14) Epinephrine injection – emergency anaphylaxis treatment. Not routine, but important if a severe allergic reaction occurs to medicines/latex/etc. Class: adrenergic agonist. Dose/time: emergency protocols; clinician. Purpose: reverse life-threatening allergy. Mechanism: opens airways and supports blood pressure. Side effects: fast heartbeat, tremor, anxiety sensations. FDA Access Data+1

15) Prednisone – steroid anti-inflammatory (selected cases). Not routine for syndactyly, but sometimes used for strong inflammation or allergic reactions when a clinician decides it is needed. Class: corticosteroid. Dose/time: clinician per label. Purpose: reduce swelling/inflammation. Mechanism: changes immune signaling and inflammatory gene activity. Side effects: mood changes, high sugar, infection risk with longer use. FDA Access Data+1

16) Cefazolin (IV) – antibiotic often used around surgery. Frequently used as surgical prophylaxis by hospitals. Class: cephalosporin antibiotic. Dose/time: clinician per label and procedure protocols. Purpose: prevent/treat skin and soft-tissue bacteria. Mechanism: blocks bacterial cell wall building. Side effects: allergy, diarrhea; rare severe reactions. FDA Access Data+1

17) Clindamycin (IV/PO) – antibiotic option for some allergies. Sometimes used if a patient cannot take beta-lactams or for certain bacteria. Class: lincosamide antibiotic. Dose/time: clinician per label. Purpose: treat susceptible infections. Mechanism: blocks bacterial protein production. Side effects: diarrhea and serious colitis risk (C. difficile), rash. FDA Access Data+1

18) Cephalexin (Keflex) – oral antibiotic for skin infections. Sometimes used for mild post-op skin infections or prophylaxis per clinician. Class: cephalosporin. Dose/time: label-based by clinician. Purpose: treat skin/soft-tissue infections. Mechanism: blocks bacterial cell wall formation. Side effects: allergy, stomach upset, diarrhea. FDA Access Data+1

19) Amoxicillin/clavulanate (Augmentin) – broad oral antibiotic. Used when broader coverage is needed (clinician decision). Class: penicillin antibiotic + beta-lactamase inhibitor. Dose/time: label-based, weight and age considered. Purpose: treat mixed bacterial infections. Mechanism: kills bacteria via cell wall inhibition; clavulanate blocks resistance enzymes. Side effects: diarrhea, rash, allergy. FDA Access Data+1

20) Mupirocin (Bactroban) – topical antibiotic. Used for certain skin infections (not deep surgical infections). Class: topical antibacterial. Dose/time: label-based. Purpose: reduce superficial bacterial growth. Mechanism: blocks bacterial isoleucyl-tRNA synthetase (stops protein building). Side effects: local burning/irritation; avoid inappropriate long use. FDA Access Data+1


Dietary molecular supplements

Important: Supplements cannot correct fused bones/skin, but some may support general nutrition and healing, especially after surgery, if a clinician agrees. Office of Dietary Supplements+1

1) Vitamin D. Often used if levels are low. Dosage: commonly measured in IU and chosen by clinician based on blood level. Function: supports bone and muscle health. Mechanism: helps calcium absorption and bone remodeling. Too much can be harmful, so avoid high-dose self-use. Office of Dietary Supplements+1

2) Calcium. Helpful when diet is low in calcium or during bone growth, especially if recommended by a clinician. Dosage: depends on age and diet. Function: bone and tooth structure. Mechanism: provides mineral for bone formation and signaling. Too much can cause constipation or kidney stone risk in some people. Office of Dietary Supplements+1

3) Vitamin C. Dosage: varies; avoid mega-doses without medical advice. Function: collagen formation and antioxidant roles. Mechanism: required for collagen cross-linking in wound healing. High doses can cause stomach upset and may raise kidney stone risk in some. Office of Dietary Supplements

4) Zinc. Dosage: clinician-guided; avoid long-term high doses. Function: immune function and tissue repair. Mechanism: supports enzymes used in cell growth and wound repair. Excess zinc can cause nausea and can reduce copper absorption. Office of Dietary Supplements

5) Omega-3 fatty acids (fish oil). Dosage: product-specific; discuss if surgery is planned. Function: supports heart and may influence inflammation balance. Mechanism: changes cell membrane fatty acids and inflammatory mediator production. Side effects: stomach upset; can interact with bleeding risk in some settings. Office of Dietary Supplements

6) Magnesium. Dosage: depends on age and diet. Function: muscle and nerve function, energy metabolism. Mechanism: cofactor in many enzymes; supports normal muscle relaxation. High supplemental doses can cause diarrhea; caution with kidney disease. Office of Dietary Supplements

7) Probiotics. Dosage: depends on strain and product. Function: supports gut microbiome, sometimes helpful during/after antibiotics. Mechanism: beneficial bacteria may reduce antibiotic-associated diarrhea risk in some people. Safety: special caution in severely immunocompromised patients. Office of Dietary Supplements

8) Collagen peptides. Dosage: commonly grams/day depending on product. Function: may support skin/tissue repair in some studies. Mechanism: provides amino acids and may stimulate collagen pathways. Evidence is still developing; choose quality-tested products and do not replace medical wound care. JDD Online+1

9) Protein supplement (whey/plant protein) if diet is low. Dosage: depends on body size and diet. Function: building blocks for healing and muscle strength. Mechanism: amino acids support tissue repair and therapy gains. Use food first when possible; consider allergies and kidney issues. Office of Dietary Supplements+1

10) Iron (only if deficient). Dosage: clinician-guided after a blood test. Function: supports oxygen delivery and energy. Mechanism: needed for hemoglobin; deficiency can slow healing and cause fatigue. Too much is harmful, so avoid taking iron “just in case.” Office of Dietary Supplements+1


Drugs for immunity booster / regenerative / stem cell

There are no FDA-approved “stem cell drugs” that fix syndactyly type 7, and “immunity boosters” are not routine treatment. What clinicians may use (when appropriate) are supportive medicines for infection risk, inflammation, or wound healing in specific situations. PMC+1

1) Cefazolin (peri-operative infection prevention). Dosage: clinician sets IV dose by weight/age and hospital protocol. Function: lowers surgical infection risk. Mechanism: kills susceptible bacteria by stopping cell wall building. This supports healing indirectly by preventing infection complications. FDA Access Data+1

2) Clindamycin (alternative antibiotic if needed). Dosage: clinician per label and infection type. Function: treats certain bacteria when chosen appropriately. Mechanism: blocks bacterial protein production. It is not a “booster,” but infection control supports recovery. FDA Access Data+1

3) Mupirocin (topical antibacterial for limited skin infection). Dosage: clinician/pharmacist instructions per label. Function: helps treat specific superficial infections. Mechanism: blocks bacterial protein synthesis enzyme. Not for deep infections; used only when appropriate. FDA Access Data+1

4) Prednisone (short course for strong inflammation/allergy—selected cases). Dosage: clinician decides and tapers if needed. Function: reduces harmful inflammation that can worsen swelling or allergic reactions. Mechanism: changes immune signaling and reduces inflammatory mediators. Long-term use can increase infection risk. FDA Access Data+1

5) Epinephrine (emergency allergy rescue). Dosage: emergency clinician protocol. Function: life-saving support during anaphylaxis. Mechanism: supports blood pressure and opens airways via adrenergic receptors. Not a daily medicine, but critical safety backup in rare severe reactions. FDA Access Data+1

6) Lidocaine/Bupivacaine (local anesthesia to enable surgery/therapy). Dosage: clinician-calculated. Function: enables safer procedures and early movement by controlling pain. Mechanism: sodium channel blockade stops pain signals. These are not regenerative drugs, but good anesthesia can improve rehab participation and recovery. FDA Access Data+1


Surgeries (procedures and why they are done)

1) Syndactyly release (finger separation). Procedure: surgeon separates fused digits and rebuilds the web space. Why: improve grasp, pinch, and finger growth direction. It is planned carefully to protect blood supply, especially in complex cases. GOSH Hospital site+1

2) Z-plasty / multi-flap web reconstruction. Procedure: uses zig-zag skin flaps to create a deeper web space. Why: reduce tight straight scars and lower “web creep.” Mechanism: flap geometry spreads tension and improves web depth. thieme-connect.de+1

3) Skin grafting. Procedure: places skin (often from another site) to cover areas after separation. Why: when there is not enough local skin to cover newly exposed sides of fingers. It helps protect tendons and allows healing. PMC+1

4) Bone separation/reconstruction (osteotomy, correction of shared bones). Procedure: cuts/repositions abnormal bone connections when present. Why: improve alignment, rotation, and function in complex syndactyly with bony fusion or forearm involvement. This is individualized and may need staged operations. Genetic Diseases Info Center+1

5) Revision surgery (for web creep, scar contracture, or growth changes). Procedure: repeat web reconstruction or scar release later. Why: as the child grows, scars may tighten and the web can “climb” forward again; some patients need another surgery for best function/appearance. Washington University Orthopedics+1


Preventions

1) You cannot “prevent” the gene cause after conception, but you can prevent delays in care by early referral to specialists. NCBI+1

2) Genetic counseling before future pregnancies can reduce surprises and help planning. NCBI+1

3) Avoid harmful exposures in pregnancy (alcohol, smoking, unprescribed drugs) to reduce other birth risks (not specific to type 7, but good practice). assh.org+1

4) Early functional therapy helps prevent stiffness and learned non-use. PMC

5) Follow safe timing for surgery when recommended to prevent growth pulling and deformity. PMC+1

6) Protect the hand from injury (gloves, safe tools) to prevent skin breaks and infection. assh.org

7) Good wound care after surgery prevents infection and graft failure. GOSH Hospital site+1

8) Do not mix NSAIDs (like ibuprofen + naproxen) unless a clinician says—this prevents bleeding/stomach harm. FDA Access Data+1

9) Count total acetaminophen from all products to prevent overdose. FDA Access Data+1

10) Keep follow-up visits to catch web creep or contractures early. Washington University Orthopedics+1


When to see a doctor

See a doctor (preferably a hand specialist) if a child has joined fingers, trouble using the hand, or forearm motion problems, because early assessment helps long-term planning. assh.org+1

Seek urgent care if there is severe pain, swelling, fever, spreading redness, pus, bad smell from a wound, new numbness, blue/cold fingers, or vomiting that will not stop after surgery/anesthesia—these can be warning signs of infection or circulation problems. GOSH Hospital site+2FDA Access Data+2

If any strong pain medicine is used (especially opioids), urgent help is needed for extreme sleepiness, slow breathing, or confusion, because breathing suppression is a known serious risk. FDA Access Data+1


What to eat and what to avoid

1) Eat: protein at each meal (eggs, fish, beans, yogurt) for tissue repair. Avoid: skipping meals after surgery. Office of Dietary Supplements+1

2) Eat: vitamin-C foods (citrus, guava, peppers) to support collagen. Avoid: very high-dose vitamin C without advice. Office of Dietary Supplements

3) Eat: calcium foods (milk, yogurt, leafy greens) for bones. Avoid: relying on supplements if diet is already strong unless advised. Office of Dietary Supplements

4) Eat: vitamin-D sources (fortified foods, safe sun, clinician-guided supplements). Avoid: high-dose vitamin D “mega dosing.” Office of Dietary Supplements+1

5) Eat: zinc sources (meat, legumes, nuts) for healing. Avoid: long-term high-dose zinc supplements. Office of Dietary Supplements

6) Eat: fiber + water to prevent constipation, especially if pain medicines are used. Avoid: low-fiber fast-food-only patterns during recovery. FDA Access Data+1

7) Eat: omega-3 foods (fish) if tolerated. Avoid: starting fish-oil supplements right before surgery unless the surgical team agrees. Office of Dietary Supplements

8) Eat: fruits/vegetables for micronutrients. Avoid: excess sugary drinks that can worsen inflammation and energy crashes. Office of Dietary Supplements+1

9) Eat: probiotic foods (yogurt, fermented foods) if appropriate. Avoid: random probiotic pills in high-risk patients without clinician input. Office of Dietary Supplements

10) Avoid: smoking/vaping exposure (even secondhand) because it can slow healing. Choose clean air and good sleep. PMC+1

FAQs

1) Is syndactyly type 7 the same as “regular syndactyly”? It is a syndactyly, but type 7 is often more complex and can involve bones and forearm changes. Genetic Diseases Info Center+1

2) What is another name for syndactyly type 7? It is commonly linked with Cenani–Lenz syndactyly syndrome. Orpha.net+1

3) Did the parents cause it? Usually no. It is commonly genetic (often recessive), not caused by parenting. NCBI+1

4) Can medicine fix the fused fingers? No. Drugs can help pain, nausea, or infection, but they do not separate fingers. PMC+1

5) What is the main treatment? When needed, surgery plus therapy is the main approach. GOSH Hospital site+1

6) When is surgery done? Timing depends on which fingers are fused and how complex it is; many surgeons operate in early childhood, sometimes earlier for certain digits. PMC+1

7) Is more than one surgery common? It can be, especially in complex cases or if web creep happens during growth. Washington University Orthopedics+1

8) Will the hand be “normal” after surgery? Surgery can improve function and appearance, but complex syndactyly may still have limits, especially if bones are involved. PMC+1

9) Is therapy really necessary? Yes—therapy helps stiffness, strength, and skill learning before and after surgery. PMC+1

10) Can the fused area come back? Skin can tighten or the web can creep forward again as the child grows; follow-up helps catch this early. Washington University Orthopedics+1

11) Are opioids always needed after surgery? Not always. Many plans start with acetaminophen/NSAIDs and add stronger medicines only if needed and safe. FDA Access Data+2FDA Access Data+2

12) Are antibiotics always needed? Not always. Some antibiotics are used around surgery or when infection is suspected, based on clinician judgment. FDA Access Data+1

13) Do supplements help? They can support nutrition if there is a deficiency, but they do not correct the hand structure. Office of Dietary Supplements+1

14) Are stem cell treatments available for this? There are no FDA-approved stem cell drugs that repair syndactyly type 7; be cautious with clinics making strong claims. PMC+1

15) What specialist should we see first? A pediatric hand/upper-limb surgeon (often in plastic surgery or orthopedics) plus OT/hand therapy is a strong starting point. assh.org+1

Disclaimer: Each person’s journey is unique, treatment plan, life style, food habit, hormonal condition, immune system, chronic disease condition, geological location, weather and previous medical  history is also unique. So always seek the best advice from a qualified medical professional or health care provider before trying any treatments to ensure to find out the best plan for you. This guide is for general information and educational purposes only. Regular check-ups and awareness can help to manage and prevent complications associated with these diseases conditions. If you or someone are suffering from this disease condition bookmark this website or share with someone who might find it useful! Boost your knowledge and stay ahead in your health journey. We always try to ensure that the content is regularly updated to reflect the latest medical research and treatment options. Thank you for giving your valuable time to read the article.

The article is written by Team RxHarun and reviewed by the Rx Editorial Board Members

Last Updated: December 16, 2025.

PDF Documents For This Disease Condition

  1. Rare Diseases and Medical Genetics.[rxharun.com]
  2. i2023_IFPMA_Rare_Diseases_Brochure_28Feb2017_FINAL.[rxharun.com]
  3. the-UK-rare-diseases-framework.[rxharun.com]
  4. National-Recommendations-for-Rare-Disease-Health-Care-Summary.[rxharun.com]
  5. History of rare diseases and their genetic.[rxharun.com]
  6. health-care-and-rare-disorders.[rxharun.com]
  7. Rare Disease Registries.[rxharun.com]
  8. autoimmune-Rare-Genetic-Diseases.[rxharun.com]
  9. Rare Genetic Diseases.[rxharun.com]
  10. rare-disease-day.[rxharun.com]
  11. Rare_Disease_Drugs_e.[rxharun.com]
  12. fda-CDER-Rare-Diseases-Public-Workshop-Master.[rxharun.com]
  13. rare-and-inherited-disease-eligibility-criteria.[rxharun.com]
  14. FDA-rare-disease-list.pdf-rxharun.com1 Human-Gene-Therapy-for-Rare Diseases_Jan_2020fda.[rxharun.com]
  15. FDA-rare-disease-lists.[rxharun.com]
  16. 30212783fnl_Rare Disease.[rxharun.com]
  17. FDA-rare-disease-list.[rxharun.com]
  18. List of rare disease.[rxharun.com]
  19. Genome Res.-2025-Steyaert-755-68.[rxharun.com]
  20. uk-practice-guidelines-for-variant-classification-v4-01-2020.[rxharun.com]
  21. PIIS2949774424010355.[rxharun.com]
  22. hidden-costs-2016.[rxharun.com]
  23. B156_CONF2-en.[rxharun.com]
  24. IRDiRC_State-of-Play-2018_Final.[rxharun.com]
  25. IRDR_2022Vol11No3_pp96_160.[rxharun.com]
  26. from-orphan-to-opportunity-mastering-rare-disease-launch-excellence.[rxharun.com]
  27. Rare disease fda.[rxharun.com]
  28. England-Rare-Diseases-Action-Plan-2022.[rxharun.com]
  29. SCRDAC 2024 Report.[rxharun.com]
  30. CORD-Rare-Disease-Survey_Full-Report_Feb-2870-2.[rxharun.com]
  31. Stats-behind-the-stories-Genetic-Alliance-UK-2024.[rxharun.com]
  32. rare-and-inherited-disease-eligibility-criteria-v2.[rxharun.com]
  33. ENG_White paper_A4_Digital_FINAL.[rxharun.com]
  34. UK_Strategy_for_Rare_Diseases.[rxharun.com]
  35. MalaysiaRareDiseaseList.[rxharun.com]
  36. EURORDISCARE_FULLBOOKr.[rxharun.com]
  37. EMHJ_1999_5_6_1104_1113.[rxharun.com]
  38. national-genomic-test-directory-rare-and-inherited-disease-eligibilitycriteria-.[rxharun.com]
  39. be-counted-052722-WEB.[rxharun.com]
  40. RDI-Resource-Map-AMR_MARCH-2024.[rxharun.com]
  41. genomic-analysis-of-rare-disease-brochure.[rxharun.com]
  42. List-of-rare-diseases.[rxharun.com]
  43. RDI-Resource-Map-AFROEMRO_APRIL[rxharun.com]
  44. rdnumbers.[rxharun.com] .
  45. Rare disease atoz .[rxharun.com]
  46. EmanPublisher_12_5830biosciences-.[rxharun.com]

References

  1. https://www.ncbi.nlm.nih.gov/books/NBK208609/
  2. https://pmc.ncbi.nlm.nih.gov/articles/PMC6279436/
  3. https://rarediseases.org/rare-diseases/
  4. https://rarediseases.info.nih.gov/diseases
  5. https://en.wikipedia.org/w/index.php?title=Category:Rare_diseases
  6. https://en.wikipedia.org/wiki/List_of_genetic_disorders
  7. https://en.wikipedia.org/wiki/Category:Genetic_diseases_and_disorders
  8. https://medlineplus.gov/genetics/condition/
  9. https://geneticalliance.org.uk/support-and-information/a-z-of-genetic-and-rare-conditions/
  10. https://www.fda.gov/patients/rare-diseases-fda
  11. https://www.fda.gov/science-research/clinical-trials-and-human-subject-protection/support-clinical-trials-advancing-rare-disease-therapeutics-start-pilot-program
  12. https://accp1.onlinelibrary.wiley.com/doi/full/10.1002/jcph.2134
  13. https://www.mayoclinicproceedings.org/article/S0025-6196%2823%2900116-7/fulltext
  14. https://www.ncbi.nlm.nih.gov/mesh?
  15. https://www.rarediseasesinternational.org/working-with-the-who/
  16. https://ojrd.biomedcentral.com/articles/10.1186/s13023-024-03322-7
  17. https://www.rarediseasesnetwork.org/
  18. https://www.cancer.gov/publications/dictionaries/cancer-terms/def/rare-disease
  19. https://www.raregenomics.org/rare-disease-list
  20. https://www.astrazeneca.com/our-therapy-areas/rare-disease.html
  21. https://bioresource.nihr.ac.uk/rare
  22. https://www.roche.com/solutions/focus-areas/neuroscience/rare-diseases
  23. https://geneticalliance.org.uk/support-and-information/a-z-of-genetic-and-rare-conditions/
  24. https://www.genomicsengland.co.uk/genomic-medicine/understanding-genomics/rare-disease-genomics
  25. https://www.oxfordhealth.nhs.uk/cit/resources/genetic-rare-disorders/
  26. https://genomemedicine.biomedcentral.com/articles/10.1186/s13073-022-01026
  27. https://wikicure.fandom.com/wiki/Rare_Diseases
  28. https://www.wikidoc.org/index.php/List_of_genetic_disorders
  29. https://www.medschool.umaryland.edu/btbank/investigators/list-of-disorders/
  30. https://www.orpha.net/en/disease/list
  31. https://www.genetics.edu.au/SitePages/A-Z-genetic-conditions.aspx
  32. https://ojrd.biomedcentral.com/
  33. https://health.ec.europa.eu/rare-diseases-and-european-reference-networks/rare-diseases_en
  34. https://bioportal.bioontology.org/ontologies/ORDO
  35. https://www.orpha.net/en/disease/list
  36. https://www.fda.gov/industry/medical-products-rare-diseases-and-conditions
  37. https://www.gao.gov/products/gao-25-106774
  38. https://www.gene.com/partners/what-we-are-looking-for/rare-diseases
  39. https://www.genome.gov/For-Patients-and-Families/Genetic-Disorders
  40. https://geneticalliance.org.uk/support-and-information/a-z-of-genetic-and-rare-conditions/
  41. https://my.clevelandclinic.org/health/diseases/21751-genetic-disorders
  42. https://globalgenes.org/rare-disease-facts/
  43. https://www.nidcd.nih.gov/directory/national-organization-rare-disorders-nord
  44. https://byjus.com/biology/genetic-disorders/
  45. https://www.cdc.gov/genomics-and-health/about/genetic-disorders.html
  46. https://www.genomicseducation.hee.nhs.uk/doc-type/genetic-conditions/
  47. https://www.thegenehome.com/basics-of-genetics/disease-examples
  48. https://www.oxfordhealth.nhs.uk/cit/resources/genetic-rare-disorders/
  49. https://www.pfizerclinicaltrials.com/our-research/rare-diseases
  50. https://clinicaltrials.gov/ct2/results?recrs
  51. https://apps.who.int/gb/ebwha/pdf_files/EB116/B116_3-en.pdf
  52. https://stemcellsjournals.onlinelibrary.wiley.com/doi/10.1002/sctm.21-0239
  53. https://www.nibib.nih.gov/
  54. https://www.nei.nih.gov/
  55. https://oxfordtreatment.com/
  56. https://www.nidcd.nih.gov/health/https://consumer.ftc.gov/articles/
  57. https://www.nccih.nih.gov/health
  58. https://catalog.ninds.nih.gov/
  59. https://www.aarda.org/diseaselist/
  60. https://www.ninds.nih.gov/Disorders/Patient-Caregiver-Education/Fact-Sheets
  61. https://www.nibib.nih.gov/
  62. https://www.nia.nih.gov/health/topics
  63. https://www.nichd.nih.gov/
  64. https://www.nimh.nih.gov/health/topics
  65. https://www.nichd.nih.gov/
  66. https://www.niehs.nih.gov/
  67. https://www.nimhd.nih.gov/
  68. https://www.nhlbi.nih.gov/health-topics
  69. https://obssr.od.nih.gov/.
  70. https://www.nichd.nih.gov/health/topics
  71. https://rarediseases.info.nih.gov/diseases
  72. https://beta.rarediseases.info.nih.gov/diseases
  73. https://orwh.od.nih.gov/

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