Marie-Sainton disease is another name for a rare bone and tooth disorder officially called cleidocranial dysplasia or cleidocranial dysostosis. In this disease, some bones do not form properly, especially the skull, collarbones (clavicles), face, teeth and sometimes the spine and pelvis.
Marie-Sainton disease is another name for cleidocranial dysplasia (cleidocranial dysostosis), a genetic bone-development condition most often caused by changes in the RUNX2 gene. It mainly affects skull bone closure, collarbones (clavicles), teeth development, and overall bone growth, so people may have a soft or delayed-closing skull, very flexible shoulders, short stature, dental crowding, and extra or delayed teeth. It is usually inherited in an autosomal dominant way, meaning one changed gene copy can cause the condition, but some people are the first in their family to have it. 1
The problem is present from birth and happens because of a change in a gene that controls how bone-forming cells work. Most people with Marie-Sainton disease have normal intelligence and a normal life span, but they may be shorter than others and can have many dental and skeletal problems that need lifelong follow-up and treatment.
Other names
Doctors use several names for the same condition. “Marie-Sainton disease” is a historic name after the early doctors who described it. Other names include cleidocranial dysplasia (CCD), cleidocranial dysostosis, Scheuthauer-Marie-Sainton syndrome and mutational dysostosis. All of these names describe one main disorder that affects the collarbones, skull, face and teeth.
Types of Marie-Sainton disease
There is only one main disease, but doctors sometimes describe “types” or “forms” based on how strong the signs are. These are not official genetic subtypes, but they help explain what a patient looks like in daily life.
-
Typical (classic) form – This is the most common form. People have open skull sutures and fontanelles, under-developed or missing collarbones, short height and clear dental problems like many extra teeth and very late tooth eruption.
-
Mild or attenuated form – In this form, signs are softer. A person may have only mild skull or dental changes and almost normal collarbones. The disease may be found only when dental X-rays or family screening are done.
-
Severe form – Some people have very wide open skull sutures, no collarbones at all, very narrow shoulders, many extra teeth and marked spine and pelvic changes. They may need more surgeries and dental work.
-
Isolated dental-predominant form – A few patients mainly show dental signs, such as delayed eruption and extra teeth, while body and skull bones are less obviously affected. Genetic testing can still show the same gene change as in the classic form.
-
Familial vs. de novo forms – Some families have many affected members across generations (familial form). In other people, the disease appears for the first time in a child, with no earlier family history (de novo form), even though the underlying gene change is the same type.
Causes of Marie-Sainton disease
Marie-Sainton disease has one main basic cause: a change (mutation) in a bone-control gene called RUNX2. The 20 “causes” below are different ways this gene change can appear or be passed on, and different factors linked to how strong the disease looks.
-
Loss-of-function mutation in RUNX2 gene – In most patients, one copy of the RUNX2 gene does not work well. This gene controls how stem cells become bone-forming cells (osteoblasts). When one copy is faulty, bone building is delayed or incomplete.
-
Autosomal dominant inheritance – The condition usually follows an autosomal dominant pattern. This means one changed gene from an affected parent is enough to cause the disease in the child, with a 50% chance in each pregnancy.
-
De novo (new) mutation in the child – In many cases, neither parent seems affected. The gene change first appears in the egg or sperm or early embryo, causing the disease in that child even when the family has no history.
-
Germline mosaicism in a parent – Rarely, a parent carries the RUNX2 mutation in some egg or sperm cells but not in their body cells, so they look normal but can have more than one affected child.
-
Large deletions involving the RUNX2 region – Sometimes a piece of chromosome 6 that contains all or part of the RUNX2 gene is missing. This loss reduces gene dose and leads to the same bone and dental problems.
-
Small insertions or deletions (indels) in RUNX2 – Very small gains or losses of DNA letters can disrupt the run of the gene, change the reading frame and produce a shortened, non-working protein.
-
Missense variants in RUNX2 – In some patients, only one amino acid in the protein changes. Even this small change can distort the shape of the RUNX2 protein and weaken its ability to turn bone genes on.
-
Nonsense variants in RUNX2 – A nonsense mutation adds a “stop” signal too early in the gene. The protein stops being built and becomes short and weak or is destroyed by the cell.
-
Splice-site mutations – Some variants affect the places where the cell cuts and joins the RNA message. This can lead to missing or extra pieces in the final RUNX2 message, again reducing its function.
-
Mutations in gene control regions – A few patients have changes in promoter or enhancer regions that control how strongly RUNX2 is used, leading to low gene activity even when the coding region looks normal.
-
Genetic heterogeneity (other genes, such as CBFB) – Very rarely, a similar cleidocranial-like picture can be linked to changes in another gene such as CBFB, which partners with RUNX2 in bone development.
-
Family clustering of skeletal dysplasia – When many family members across generations show similar bone and dental signs, this clustering reflects the inherited gene change, even if it has not yet been identified in the lab.
-
Modifier genes – Other genes that affect bone density, tooth formation or hormone action may modify how severe Marie-Sainton disease looks, making some people mild and others more affected, even with similar RUNX2 changes.
-
Epigenetic changes – Chemical marks on DNA or histones may change how well the RUNX2 gene is read. This does not cause the disease by itself but may influence severity in people who already have a mutation.
-
Copy-number variation around RUNX2 – Extra copies or losses near the RUNX2 gene may disturb its dosage or long-range control and be linked to Marie-Sainton-like features in some patients.
-
Advanced parental age (for de novo mutations in general) – In many genetic conditions, new mutations are slightly more common when one parent, often the father, is older. For Marie-Sainton disease this is not clearly proven, but it may play a small role in some new cases.
-
Unknown genetic changes (mutation not yet found) – A small number of patients show a classic clinical picture, but current tests do not find a clear gene change. This suggests there are still unknown changes or mechanisms that can disturb RUNX2 pathways.
-
Environmental influences on bone growth in the fetus – Certain environmental or nutritional issues in early pregnancy might slightly modify how bones form in a fetus that already carries a RUNX2 change, but they are not the main cause of the disease.
-
Reduced penetrance in some carriers – Some people inherit the mutation but have very mild or almost no visible signs. This “reduced penetrance” can hide the gene in a family and then appear more strongly in a child.
-
Random chance in genetic transmission – Because of autosomal dominant inheritance, each child of an affected parent has a 50% chance to receive the changed gene. Which child is affected is largely due to chance, not to anything the parents did or did not do.
Symptoms of Marie-Sainton disease
Symptoms can be very different from person to person, even inside the same family. Below are 15 common symptoms explained in simple words.
-
Open fontanelles and wide skull sutures – The soft spots on the baby’s head (fontanelles) stay open for a long time and the lines between skull bones (sutures) remain wide. This happens because the skull bones form and join more slowly than normal.
-
Prominent forehead (frontal bossing) – The forehead often looks big and sticks out more than usual. This is due to the abnormal growth pattern of the skull bones and the delayed closure of the top of the skull.
-
Flat midface and depressed nasal bridge – The middle part of the face, including the upper jaw and nose area, can be under-developed. The bridge of the nose may look flat, and the face may seem “sunken” in the middle.
-
Under-developed or missing collarbones – Collarbones can be short, thin or even completely absent. Because of this, the shoulders look narrow and can be brought very close together in front of the chest, which is a classic sign of this disease.
-
Narrow, sloping shoulders and chest changes – The shoulders often slope down and the upper chest may look narrow. Some people have extra ribs or unusual rib shapes, which can slightly change the shape of the chest wall.
-
Short stature – Many children and adults are shorter than average. The long bones of the arms and legs grow more slowly, so height is reduced, but body proportions are usually near normal.
-
Dental crowding and delayed eruption – Baby teeth may fall out late and adult teeth may come in very late or not at all. The jaws can be crowded, making it hard for teeth to line up properly and often causing bite problems.
-
Extra teeth (supernumerary teeth) – Many people develop far more teeth than normal, especially in the upper jaw. These extra teeth are often stuck inside the jaw bone and can block normal teeth from erupting.
-
Jaw and bite problems (malocclusion) – Because of extra and delayed teeth and the small upper jaw, the bite may not line up. This can cause chewing trouble, jaw pain and cosmetic concerns, and often needs orthodontic and surgical correction.
-
Recurrent sinus and ear infections – Abnormal facial bones and crowded teeth can change the drainage of the nose and sinuses. Some children have frequent sinus or ear infections and may need ENT (ear, nose, throat) care.
-
Hearing loss – Conductive hearing loss can occur because the tiny bones of the middle ear and nearby skull structures are affected. Fluid or repeated ear infections may also add to hearing problems.
-
Spine problems (scoliosis or kyphosis) – Some patients develop sideways bending of the spine (scoliosis) or a round-back posture (kyphosis). These spine curves may cause back pain and need monitoring, bracing or surgery.
-
Wide pelvis and hip issues – The pelvic bones can be wide and sometimes shaped differently. This may cause hip problems such as coxa vara (changed angle of the upper thigh bone) and can affect walking or childbirth in adults.
-
Hand and finger changes – Shortened fingers, especially the middle bone of the little finger, and other hand bone changes are common. These are usually painless but help doctors recognise the condition on X-rays.
-
Fatigue, aches and body image concerns – Many people feel tired or have aches in the back, shoulders or jaw after activity because their bones and muscles work in a slightly unusual way. Changes in appearance can also affect confidence and mood.
Diagnostic tests for Marie-Sainton disease
Doctors use a mix of physical exam, manual tests, lab tests, electrodiagnostic tests and imaging to confirm the diagnosis and plan treatment. Genetic testing helps confirm the exact gene change, but the diagnosis is often suspected first from the way the person looks and their X-rays.
Physical examination tests
-
Comprehensive physical examination – The doctor looks at the whole body, checks height, weight, head size and body shape, and looks for open skull sutures, shoulder shape and chest and spine curves. This first exam gives a strong clue to the diagnosis.
-
Growth and anthropometric measurements – The doctor measures height, arm span, sitting height, head circumference and shoulder width. These numbers are compared with age charts to see if the child is small for age and if body parts are in normal proportion.
-
Skull and fontanelle examination – The scalp is gently felt to check whether the fontanelles (soft spots) are still open and if skull sutures are wide. A large, soft area or many small bone islands (Wormian bones) suggest Marie-Sainton disease.
-
Clavicle and shoulder movement test – The doctor checks if the collarbones can be felt and if the patient can bring the shoulders together in front of the chest. Very flexible shoulders or missing collarbones are a classic sign of this disease.
-
Spine and chest wall examination – The spine is viewed from the back and side while the patient stands and bends forward. The doctor looks for curves, uneven shoulders and changes in chest shape that may need imaging or treatment.
Manual tests
-
Shoulder range-of-motion assessment – Using simple movements or a measuring tool, the doctor checks how far the shoulders can move in different directions. Excess movement, though painless, supports the idea of missing or weak collarbones.
-
Posture and gait assessment – The patient is asked to stand and walk back and forth. The doctor watches the posture, spine alignment and walking style to see if spine curves or hip problems are affecting balance or movement.
-
Simple bedside hearing tests – Whisper tests and tuning-fork tests (Rinne and Weber) can quickly show if there is likely to be hearing loss. If these simple tests are abnormal, more detailed hearing studies are arranged.
Lab and pathological tests
-
RUNX2 genetic testing (single-gene test) – A blood sample is sent to look for mutations in the RUNX2 gene. Finding a harmful change confirms the diagnosis at the DNA level and can help with family counselling and planning.
-
Multigene skeletal dysplasia or exome panel – When the picture is not typical, doctors may use a panel that tests many bone-related genes or even whole exome sequencing. This helps detect rare or unusual variants linked to Marie-Sainton-like features.
-
Basic bone health blood tests – Blood tests for calcium, phosphate, alkaline phosphatase and vitamin D are done to check general bone health and to rule out other bone diseases that might mimic some signs of this condition.
-
Thyroid and parathyroid function tests – Levels of thyroid hormone and parathyroid hormone are checked to exclude hormonal causes of abnormal bone growth, making sure that the skeletal changes really come from this genetic disease.
-
Bone turnover markers or bone density-related tests – In some patients, special blood or urine tests for bone formation and breakdown markers may be ordered to study how active bone remodelling is and to guide long-term management.
Electrodiagnostic and audiologic tests
-
Pure-tone audiometry – This hearing test uses headphones and different sound tones to measure how softly a person can hear each frequency. It helps show if a patient has conductive hearing loss, which is common in Marie-Sainton disease.
-
Tympanometry and middle-ear function tests – A small probe in the ear canal measures how the eardrum moves. This shows fluid, stiffness or pressure problems in the middle ear, which may explain hearing loss in affected patients.
-
Nerve conduction studies and EMG (if nerve compression is suspected) – In rare cases where collarbone fragments irritate nearby nerves, tests that measure nerve conduction and muscle activity can show if a nerve is being compressed and needs surgical help.
Imaging tests
-
X-ray of skull and facial bones – Skull X-rays show wide open sutures, open fontanelles, Wormian bones and under-developed facial bones. These features are very typical and help confirm the diagnosis along with the physical signs.
-
X-ray of chest and clavicles – A chest X-ray clearly shows the collarbones and ribs. It may reveal short, thin or missing clavicles, extra ribs or other chest bone changes that strongly suggest Marie-Sainton disease.
-
Panoramic dental X-ray (orthopantomogram) – This wide dental X-ray shows all teeth and jaw bones. It often reveals many extra teeth, impacted teeth and abnormal tooth shapes, which are hallmarks of the condition.
-
X-rays of spine, pelvis and long bones – X-rays of the spine and pelvis show curves and hip angles, while images of the hands and long bones show typical bone shapes. Together with skull and chest films, they give a full skeletal overview.
-
CT scan or 3D imaging of skull and chest (when needed) – In complex cases, CT or 3D imaging can give very detailed pictures of skull, jaw, ear bones and collarbones. This helps surgeons plan operations on the face, teeth or chest safely and precisely.
Non-pharmacological treatments
-
Coordinated “team care” plan: Care works best when a dentist/orthodontist, oral surgeon, ENT, and orthopedic specialist follow one plan, because tooth, jaw, airway, and posture issues are connected. Purpose: fewer missed problems. Mechanism: early checks catch delayed tooth eruption, bite problems, scoliosis, and hearing issues before they become harder to fix. 1
-
Early dental monitoring (childhood onward): Regular dental X-rays and exams help track delayed or extra teeth. Purpose: protect chewing, speech, and facial growth. Mechanism: knowing where teeth are “stuck” helps the dentist plan exposure, traction, or removal at the safest time. 1
-
Orthodontic alignment therapy: Braces or aligners may be needed longer than usual. Purpose: improve bite and appearance and reduce gum injury from crowding. Mechanism: slow, controlled tooth movement makes room and guides erupting teeth into better positions. 3
-
Surgical-orthodontic “expose and pull” technique: A dentist/oral surgeon may uncover impacted teeth and attach a chain for traction. Purpose: bring permanent teeth into the mouth instead of leaving them trapped. Mechanism: gentle pulling over months helps the tooth erupt through bone and gum. 1
-
Planned removal of extra teeth (supernumerary teeth): Extra teeth often block normal eruption. Purpose: open the path for permanent teeth. Mechanism: removing blockers reduces crowding pressure and makes orthodontic movement more predictable. 1
-
Preventive dental hygiene coaching: Careful brushing, flossing, and professional cleanings are important because crowding traps plaque. Purpose: prevent cavities and gum disease. Mechanism: less plaque means fewer bacteria, less inflammation, and fewer dental infections before surgeries or orthodontics. 3
-
Speech therapy (if needed): Some people develop speech issues from bite or palate shape. Purpose: clearer speech and confidence. Mechanism: targeted exercises retrain tongue and mouth movement and compensate for jaw/teeth differences. 3
-
Hearing evaluation and audiology support: Hearing checks help catch conductive hearing loss early. Purpose: protect learning and communication. Mechanism: early diagnosis allows timely ear care (like tubes/hearing aids) instead of long untreated hearing reduction. 1
-
ENT care for recurrent sinus/ear infections: Many patients need guided ENT follow-up. Purpose: reduce repeated infections and hearing damage. Mechanism: treating nasal blockage, allergies, or chronic fluid reduces inflammation and bacterial growth. 1
-
Posture training and core strengthening: A physiotherapist can teach posture habits. Purpose: reduce back/neck strain. Mechanism: stronger core and scapular muscles support the spine and shoulders, lowering pain from looseness and poor posture. 3
-
Scoliosis screening and bracing (when appropriate): Spine curves should be monitored. Purpose: prevent worsening curvature. Mechanism: braces guide growth and reduce curve progression during growth spurts. 1
-
Low-impact exercise routine: Walking, cycling, swimming, and light strength training are usually helpful. Purpose: build bone and muscle safely. Mechanism: regular mechanical loading signals bones and muscles to strengthen without high injury risk. 3
-
Fall-prevention and balance training: If joints are loose or posture is poor, balance work helps. Purpose: fewer injuries. Mechanism: improving proprioception (body position sense) and leg strength reduces stumbling and falls. 3
-
Ergonomic setup for study/work: Chair height, screen level, and breaks matter. Purpose: less neck/back pain. Mechanism: neutral posture reduces constant strain on muscles that already work harder to stabilize loose joints. 3
-
Pain-coping skills (CBT, relaxation, pacing): Chronic dental/orthopedic work can be stressful. Purpose: better quality of life. Mechanism: pacing and relaxation reduce pain amplification from stress and improve sleep and function. 3
-
Nutritional counseling for bone health: A dietitian can plan adequate protein, calcium, and vitamin D foods. Purpose: support bone and healing. Mechanism: bone remodeling needs minerals plus protein; good intake supports recovery after dental/orthopedic procedures. 1
-
Sleep and airway assessment: Some people have midface/jaw structure that affects breathing. Purpose: reduce poor sleep and daytime fatigue. Mechanism: identifying snoring or sleep apnea allows targeted fixes (dental devices/ENT care). 3
-
Psychological support (self-image and long treatment timelines): Long orthodontic plans can affect confidence. Purpose: protect mental well-being. Mechanism: counseling builds coping strategies and reduces treatment burnout. 3
-
Genetic counseling for family planning: Families often want clear inheritance information. Purpose: informed decisions. Mechanism: counseling explains autosomal dominant inheritance and testing options in simple terms. 2
-
Regular follow-up schedule (surveillance): Ongoing checks are key because needs change with age. Purpose: prevent surprises. Mechanism: planned intervals for dental imaging, hearing checks, and spine/orthopedic review catch new issues early. 1
Drug treatments
-
Acetaminophen (paracetamol): Often used for mild to moderate pain after dental work or for general aches. Class: analgesic/antipyretic. Dosage/time: depends on age and liver health; follow label and clinician advice. Purpose: pain/fever relief. Mechanism: acts in the central nervous system to reduce pain/fever signaling. Side effects: liver injury risk with overdose or combining products. 10
-
Ibuprofen: Useful for pain with inflammation (jaw pain, muscle aches). Class: NSAID. Dosage/time: shortest time and lowest dose that works. Purpose: reduce pain and swelling. Mechanism: lowers prostaglandins that drive inflammation. Side effects: stomach bleeding risk, kidney strain, and other NSAID warnings. 11
-
Naproxen sodium: Another NSAID option for longer-lasting pain relief. Class: NSAID. Dosage/time: follow label; avoid combining with other NSAIDs. Purpose: pain and inflammation control. Mechanism: prostaglandin reduction. Side effects: stomach bleeding and allergy risks like other NSAIDs. 12
-
Tramadol (short-term severe pain): Sometimes used when pain is not controlled by simple medicines. Class: opioid-like analgesic. Dosage/time: shortest duration possible under medical supervision. Purpose: stronger pain relief. Mechanism: affects opioid receptors and neurotransmitters. Side effects: dizziness, dependence risk, breathing risk, and seizure risk in some patients. 13
-
Oxycodone controlled-release (selected cases): Reserved for severe pain when continuous analgesia is needed. Class: opioid analgesic. Dosage/time: individualized and closely monitored. Purpose: strong pain relief. Mechanism: opioid receptor activation. Side effects: addiction/overdose risk, constipation, sedation, breathing suppression. 14
-
Lidocaine injection (local anesthetic): Common in dental procedures. Class: local anesthetic. Dosage/time: given by trained clinicians during procedures. Purpose: numb area for painless work. Mechanism: blocks nerve sodium channels so pain signals can’t travel. Side effects: toxicity if overdosed or injected into blood vessel; medical monitoring matters. 21
-
Amoxicillin: Used for dental/ear/sinus infections when bacteria are likely. Class: penicillin antibiotic. Dosage/time: depends on infection and age; complete the course. Purpose: treat bacterial infection. Mechanism: blocks bacterial cell-wall building. Side effects: diarrhea, rash, allergic reactions in sensitive people. 15
-
Amoxicillin-clavulanate: Used when bacteria may resist plain amoxicillin. Class: penicillin + beta-lactamase inhibitor. Dosage/time: take exactly as directed; often with food. Purpose: broader infection treatment. Mechanism: clavulanate blocks resistance enzymes, letting amoxicillin work. Side effects: diarrhea, stomach upset, allergy risk. 16
-
Clindamycin: Sometimes used when penicillin allergy exists (based on clinician judgment). Class: lincosamide antibiotic. Dosage/time: depends on infection; finish the course. Purpose: treat certain bacterial infections. Mechanism: blocks bacterial protein production. Side effects: diarrhea and risk of serious gut infection (C. difficile) are important warnings. 17
-
Azithromycin: Another option used for selected infections. Class: macrolide antibiotic. Dosage/time: commonly short courses. Purpose: treat susceptible bacterial infections. Mechanism: blocks bacterial protein synthesis. Side effects: stomach upset; in some people it can affect heart rhythm, so clinicians screen risk. 18
-
Cefdinir: A cephalosporin sometimes used for ear/sinus/respiratory infections. Class: cephalosporin antibiotic. Dosage/time: depends on infection; complete the course. Purpose: treat bacterial infection. Mechanism: interrupts bacterial cell-wall formation. Side effects: diarrhea, rash; allergy cross-reaction can occur in some people. 19
-
Chlorhexidine oral rinse: Often used short-term for gum inflammation or after dental procedures. Class: antiseptic rinse. Dosage/time: rinse as directed; do not swallow. Purpose: lower mouth bacteria. Mechanism: disrupts bacterial membranes and reduces plaque activity. Side effects: tooth staining and taste changes can happen. 20
-
Ondansetron (for nausea after anesthesia): Helpful after surgery for nausea/vomiting. Class: antiemetic (5-HT3 blocker). Dosage/time: peri-operative or as prescribed. Purpose: prevent vomiting and dehydration. Mechanism: blocks serotonin signaling that triggers nausea reflexes. Side effects: headache, constipation; rare rhythm issues in high-risk patients. 24
-
Dexamethasone (selected surgical swelling/inflammation): Sometimes used around surgery for swelling or severe inflammation based on clinician choice. Class: corticosteroid. Dosage/time: short-term medical use. Purpose: reduce inflammation and tissue swelling. Mechanism: suppresses inflammatory immune signals. Side effects: blood sugar rise, mood change, infection risk if prolonged. 25
-
Propofol (general anesthesia/sedation): Used by anesthesia professionals during procedures. Class: IV anesthetic. Dosage/time: in monitored medical settings only. Purpose: sedation/anesthesia. Mechanism: enhances inhibitory brain signaling to produce unconsciousness/sedation. Side effects: low blood pressure, breathing suppression—requires monitoring. 22
-
Sevoflurane (inhaled anesthesia): Common inhaled anesthetic for procedures. Class: inhaled anesthetic. Dosage/time: operating room use. Purpose: maintain anesthesia. Mechanism: alters brain signaling to maintain unconsciousness. Side effects: nausea, blood pressure changes; clinicians monitor closely. 23
-
Alendronate (bone density support—only when clinically indicated): Not for everyone with CCD, but may be used if osteoporosis/low bone density is diagnosed. Class: bisphosphonate. Dosage/time: weekly or as prescribed with strict instructions. Purpose: reduce fracture risk. Mechanism: slows bone breakdown by osteoclasts. Side effects: esophageal irritation; rare jaw bone problems—dentist should know. 26
-
Teriparatide (anabolic bone therapy—specialist only): Considered only for certain osteoporosis cases, not routine CCD care. Class: parathyroid hormone analog. Dosage/time: daily injection for limited duration. Purpose: build bone. Mechanism: stimulates new bone formation. Side effects: dizziness, calcium changes; requires clinical selection and monitoring. 27
-
Denosumab (osteoporosis therapy—selected patients): Used when fracture risk is high and a clinician chooses it. Class: RANKL inhibitor biologic. Dosage/time: injection every 6 months. Purpose: reduce bone loss and fractures. Mechanism: reduces osteoclast formation/activity. Side effects: low calcium, infections, rare jaw osteonecrosis—dental planning is important. 28
-
“Dental topical anesthetics/analgesics” (professional selection): Dentists may use topical numbing agents before injections or minor work. Class: topical anesthetics. Dosage/time: in-clinic use. Purpose: reduce procedure discomfort. Mechanism: temporary nerve signal blocking at the surface. Side effects: local irritation; dosing matters, especially in children. 21
Dietary molecular supplements
-
Vitamin D: Often used when blood levels are low or sun exposure is limited. Dosage: individualized (many people use daily low doses). Function: helps calcium absorption and bone mineralization. Mechanism: increases intestinal calcium uptake and supports bone remodeling signals. Too much can be harmful, so dose should match labs. 31
-
Calcium: Helpful if dietary calcium is low. Dosage: depends on age and total diet intake. Function: bone and teeth mineral structure. Mechanism: provides raw material for hydroxyapatite in bone; works best with vitamin D adequacy. Excess calcium can increase kidney stone risk in some people. 32
-
Vitamin C: Supports collagen formation, which is important for bone matrix and wound healing. Dosage: modest daily intake is usually enough. Function: collagen and antioxidant support. Mechanism: helps enzymes that build collagen fibers. Very high doses can cause stomach upset and are not recommended long-term. 29
-
Zinc: Sometimes used short-term if diet is poor, because zinc supports tissue repair. Dosage: avoid high chronic doses. Function: immune and wound healing support. Mechanism: supports enzyme function and immune cell signaling. Too much zinc can cause copper deficiency and neurologic problems. 30
-
Magnesium (if intake is low): Magnesium supports bone and muscle function. Dosage: based on diet and tolerance. Function: helps vitamin D and calcium metabolism. Mechanism: participates in many enzymes involved in bone turnover and muscle relaxation. Overuse can cause diarrhea. 32
-
Vitamin K (diet first; supplement only if approved): Vitamin K is involved in bone protein activation. Dosage: clinician-guided, especially if on blood thinners. Function: bone protein regulation. Mechanism: helps activate osteocalcin, a bone-related protein. Food sources are usually preferred unless advised. 32
-
Protein supplement (when diet is inadequate): Protein supports healing after dental/orthopedic procedures. Dosage: based on body size and diet. Function: tissue repair. Mechanism: provides amino acids needed for collagen, muscle, and immune repair. Choose safe, tested products if using powders. 1
-
Omega-3 (selected cases): Sometimes used for general inflammation balance. Dosage: modest, clinician-guided. Function: supports anti-inflammatory pathways. Mechanism: shifts eicosanoid production toward less inflammatory signals. Not a primary CCD therapy; think of it as general support only. 3
-
Iron (only if iron deficiency is proven): Not everyone needs iron. Dosage: based on lab results. Function: prevents anemia-related fatigue. Mechanism: restores hemoglobin building blocks. Taking iron without deficiency can cause constipation and stomach upset. 3
-
Probiotic (short term with antibiotics): Sometimes used during antibiotic courses. Dosage: varies by product. Function: gut support. Mechanism: may reduce antibiotic-associated diarrhea in some people. This is optional and should not replace completing antibiotics as prescribed. 17
Drugs (immunity support / regenerative / “stem cell” area — reality-based)
-
Denosumab (bone remodeling biologic): Not a CCD cure, but may be used for high fracture risk osteoporosis. Dosage: injection every 6 months. Function: reduces bone breakdown. Mechanism: blocks RANKL so osteoclast activity drops. Needs dental coordination because jaw complications are a known risk. 28
-
Teriparatide (bone building drug): A specialist option for severe osteoporosis. Dosage: daily injection for limited duration. Function: increases bone formation. Mechanism: intermittent PTH signaling stimulates osteoblast activity. It is “regenerative” in the sense of building bone, but it is not a gene-level CCD therapy. 27
-
Alendronate (anti-resorptive bone drug): Used when bone density is low and a clinician chooses it. Dosage: typically weekly. Function: protects bone. Mechanism: slows osteoclast-mediated bone resorption. Requires careful swallowing instructions to protect the esophagus and dental planning if surgery is expected. 26
-
Vitamin D prescription therapy (when deficiency is confirmed): Clinicians may prescribe higher-dose vitamin D for deficiency. Dosage: lab-guided. Function: supports calcium absorption and bone mineralization. Mechanism: increases calcium uptake and supports bone remodeling. Over-replacement can be dangerous, so monitoring matters. 31
-
Short-course antibiotics for infection “immune support”: When infections occur, antibiotics reduce bacterial load so the immune system can recover. Dosage: infection-specific. Function: treat bacterial infection. Mechanism: directly kills/inhibits bacteria; this is not an immune booster supplement, but it protects the body from infection harm. 15
-
Important note on “stem cell drugs”: There are no standard FDA-approved stem cell drugs that specifically treat cleidocranial dysplasia as a genetic condition; most “stem cell” approaches are investigational and must be discussed with a genetics/orthopedic specialist if ever considered. 1
Surgeries (procedures, why done)
-
Removal of extra teeth (supernumerary extraction): Done to clear the path for normal teeth and reduce crowding. It helps orthodontic traction work better and lowers infection risk from trapped teeth. 1
-
Surgical exposure of impacted permanent teeth: Done when permanent teeth do not erupt. The surgeon uncovers the tooth so orthodontics can pull it into place, improving bite and chewing. 1
-
Orthognathic (jaw) surgery (selected cases): Done for major bite problems that braces alone cannot fix. It improves chewing, speech clarity, facial balance, and sometimes airway space. 3
-
Cranial surgery (rare; only if medically necessary): Sometimes considered if skull shape causes pressure problems or severe deformity. The goal is to protect brain space and normalize head shape when needed. 1
-
Spine surgery (rare; severe scoliosis/instability): Done only when curvature is severe or progressing and threatens function. It aims to stabilize the spine and reduce pain or breathing compromise from deformity. 1
Preventions (practical ways to reduce complications)
-
Start dental follow-up early so impacted/extra teeth are found before they create major crowding. 1
-
Brush and floss carefully (crowded teeth trap plaque), and keep regular cleanings to prevent cavities before orthodontics/surgery. 3
-
Do not ignore chronic mouth pain or swelling—early treatment prevents abscesses. 3
-
Get hearing checks if you notice muffled hearing or repeated ear infections. 1
-
Maintain healthy vitamin D and calcium intake through diet and clinician-approved supplements if needed. 31
-
Exercise with low-impact activities to build strength without high injury risk. 3
-
Use good posture and ergonomics to reduce long-term back/neck strain. 3
-
Avoid smoking and second-hand smoke because it worsens gum disease and slows healing after dental work. 3
-
Follow medication labels strictly (especially pain medicines) to prevent liver injury or stomach bleeding from overdose/mixing. 10
-
Genetic counseling helps families understand inheritance and plan early screening for children. 2
When to see doctors (do not delay)
See a doctor or dentist urgently if you have face/jaw swelling, fever with tooth pain, draining pus, trouble swallowing, breathing trouble, sudden hearing loss, or severe back pain with weakness. These can signal infection, airway issues, or nerve/spine problems that need prompt care. 3
What to eat and what to avoid
-
Eat calcium-rich foods (milk/yogurt, fortified foods, leafy greens if tolerated) to support bone mineral needs. 32
-
Get vitamin D sources (safe sunlight, fortified foods, clinician-approved supplements) for calcium absorption. 31
-
Choose protein at each meal (fish, eggs, beans, lean meat) to support healing after procedures. 1
-
Eat vitamin C foods (citrus, guava, peppers) to support collagen and gum health. 29
-
Drink enough water to support overall health and reduce dry mouth (dry mouth raises cavity risk). 3
-
Limit very sugary snacks and drinks because crowding increases cavity risk. 3
-
Avoid frequent sticky foods (toffee, sticky sweets) that cling to crowded teeth and braces. 3
-
Avoid excessive soda/acidic drinks which can weaken enamel—important during long orthodontic care. 3
-
Avoid high-dose zinc long-term unless guided, because it can cause copper deficiency. 30
-
Avoid mixing multiple pain products that contain the same ingredient (like acetaminophen), because accidental overdose can happen. 10
FAQs
-
Is Marie-Sainton disease the same as cleidocranial dysplasia? Yes—Marie-Sainton disease is a name used for cleidocranial dysplasia/dysostosis. 2
-
Is it contagious? No. It is genetic, not an infection. 2
-
What gene is most commonly involved? RUNX2 is the most common gene linked to CCD. 1
-
Can a person live a normal life? Many people do, especially with good dental and orthopedic care, but they may need long-term follow-ups. 3
-
Why are the shoulders so flexible? The collarbones may be partly formed or smaller, which changes shoulder stability. 2
-
Why do teeth come late or get stuck? Extra teeth and dense bone can block normal eruption pathways. 1
-
Is there one “best” treatment? The best approach is planned, step-by-step care (dental + orthodontic + sometimes surgery) tailored to the person. 1
-
Are there FDA-approved drugs that cure CCD? No standard medicine cures the genetic cause; drugs mainly treat pain, infections, nausea, or low bone density when present. 1
-
Do all patients need surgery? No. Some need only orthodontics and monitoring; surgery depends on impacted teeth, bite problems, or severe bone issues. 3
-
Can children with CCD play sports? Often yes, but low-impact and safe strengthening is usually better; a clinician can advise based on spine/joint status. 3
-
Does CCD affect hearing? It can; hearing checks are recommended if symptoms appear. 1
-
Should I take calcium and vitamin D automatically? Not automatically—diet and blood levels matter; too much can be harmful. 31
-
What pain medicine is safest? It depends on age, stomach/kidney/liver health, and other medicines; follow labels and clinician advice and avoid mixing acetaminophen products. 10
-
Can CCD be inherited? Yes—often autosomal dominant, so it can pass from parent to child. 2
-
What specialist should coordinate care? Many people do best with a genetics or craniofacial team plus dental/orthodontic leadership, because needs change across childhood and adulthood. 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: January 31, 2025.
