Illum Syndrome

Illum syndrome is an extremely rare condition present at birth. Babies have many stiff joints (contractures), a very small, tight mouth that looks like a “whistling face,” and an almost expressionless face. Many babies also have serious brain and nervous-system problems that affect body control, saliva, temperature, breathing, and heart rate. Development is usually very delayed. Some babies have small lower jaw and airway problems (called Pierre-Robin sequence). Sadly, the condition is often life-threatening in the first months of life. Doctors believe it is part of a group called “fetal akinesia deformation sequence (FADS)”, which means the baby moved much less than normal in the womb, and that lack of movement caused the joints and face to form abnormally. Genetic Rare Disease Center+2MalaCards+2

Illum syndrome is an extremely rare condition present at birth. Babies have many stiff joints that cannot move well (called “contractures”), a very small mouth that looks like a whistling face, and a still, “mask-like” facial expression. Many babies also have serious problems with feeding, swallowing, breathing, temperature control, and sometimes seizures. Some have features of Pierre Robin sequence (small lower jaw and airway obstruction). Because of severe body system involvement, this condition can be life-limiting in the first months of life. Doctors consider it a severe form of arthrogryposis and part of the fetal akinesia (low fetal movement) spectrum. Genetic Rare Disease Center+2Orpha+2

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Other names

• Arthrogryposis multiplex congenita – whistling face syndrome

• Whistling face phenotype with generalized contractures

• ILLUM syndrome (historical synonym)
  These names point to many joint contractures (“arthrogryposis”) and the whistling-like small mouth (“microstomia”). Genetic Rare Disease Center+1

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Types

There are no official sub-types of Illum syndrome. Doctors loosely group babies by associated features and severity, for example:

1. With marked autonomic dysfunction (saliva, temperature, slow heart rate, seizures);

2. With Pierre-Robin sequence (small jaw, tongue falls back, airway trouble);

3. Lethal early course;

4. Severe but briefly survivable course. These groupings reflect how FADS-type disorders can vary from family to family. Genetic Rare Disease Center+1

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Causes

Illum syndrome sits within the fetal akinesia group—conditions where reduced fetal movement leads to contractures and facial changes. Many different upstream problems can reduce fetal movement. Below are 20 well-recognized categories/mechanisms that clinicians consider (not all apply in every child):

1. Primary brain malformations — brain areas that plan or control movement do not form normally, so the fetus moves less. autopsyandcasereports.org

2. Spinal cord/anterior horn cell disorders — motor neurons are too few or fail, lowering movement. PMC

3. Peripheral neuropathies — the nerves to muscles do not conduct signals well. PMC

4. Congenital myopathies — structural muscle diseases (e.g., myosin/actin pathway defects) make muscles weak from the start. PMC

5. Congenital myasthenic syndromes — signal transfer at the neuromuscular junction is faulty (e.g., MUSK, RAPSN, DOK7), so muscle activation is poor. Nature+1

6. Genetic variants linked to arthrogryposis — dozens of genes (e.g., PIEZO2, TGFBR1) are reported in AMC/FADS cohorts. Obstetrics & Gynecology

7. Pulmonary hypoplasia sequence — very limited movement and chest wall stiffness impair lung growth, worsening outcomes. Nature

8. Connective-tissue/contracture pathways — abnormal tendon/ligament development can “lock” joints. PMC

9. Placental or uterine constraint — severe crowding or low fluid •(oligohydramnios) reduces fetal motion. IJRCog

10. Maternal autoimmune antibodies (e.g., myasthenia gravis) — can block the baby’s neuromuscular transmission. PMC

11. Intrauterine infections (TORCH group) — damage the nervous system or muscles, lowering movement. PMC

12. Metabolic disorders — inborn errors of metabolism may weaken fetal muscles or nerves. PMC

13. Vascular disruptions — poor blood supply to developing spinal cord/nerves/muscles limits function. PMC

14. Chromosomal or syndromic disorders — some chromosomal changes include arthrogryposis in their spectrum. PMC

15. Toxic exposures — rare teratogenic effects can depress fetal neuromuscular function. PMC

16. Severe fetal growth restriction — undernourished fetuses often move less. Obstetrics & Gynecology

17. Primary autonomic dysfunction — nervous-system control of heart rate/temperature/saliva is abnormal (reported specifically in Illum syndrome). Genetic Rare Disease Center

18. Craniofacial constraint — very small mouth and jaw further limit normal oromotor movement patterns in utero. Genetic Rare Disease Center

19. Muscle structural protein variants — e.g., fetal myosin heavy chain and related genes tied to contractures. PMC

20. Idiopathic/unknown — in some babies, even with modern testing, no single cause is found. PMC

Key idea: very different starting problems can end in the same outward picture of contractures and a whistling face because too little movement in the womb causes similar body changes. PMC

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Common symptoms and signs

1. Stiff joints from birth (contractures) — elbows, knees, wrists, fingers, feet are held in fixed positions and move only a little. Genetic Rare Disease Center

2. Very small, tight mouth (microstomia) with “whistling” appearance — lips look pursed; opening the mouth is hard. Genetic Rare Disease Center

3. Expressionless face — facial muscles are weak or stiff, so expressions are limited. Genetic Rare Disease Center

4. Feeding and swallowing problems — sucking is weak; swallowing is unsafe; choking may happen. Genetic Rare Disease Center

5. Speech difficulty later — small mouth and low movement make speech development hard. Genetic Rare Disease Center

6. Excess saliva (sialorrhea) — drooling because mouth control is poor. Genetic Rare Disease Center

7. Temperature swings — the body cannot regulate heat well. Genetic Rare Disease Center

8. Seizure-like jerks (myoclonic fits) — brief shock-like movements can occur. Genetic Rare Disease Center

9. Slow heart rate (bradycardia) — due to autonomic-nervous-system problems. Genetic Rare Disease Center

10. Severe developmental delay — major delays in moving, sitting, and talking. Genetic Rare Disease Center

11. Breathing/airway trouble — some babies have small jaw and tongue-position issues (Pierre-Robin), making airway and breathing difficult. Genetic Rare Disease Center

12. Poor weight gain — feeding difficulty leads to low growth without special support. Genetic Rare Disease Center

13. Abnormal muscle tone — stiff or weak muscles on exam. Genetic Rare Disease Center

14. Calcifications in brain or muscles (reported in some cases) — seen on imaging. checkorphan.org

15. Early life-threatening course — many infants do not survive beyond the first months. Genetic Rare Disease Center

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Diagnostic tests

A) Physical examination (bedside)

1. Full newborn exam for contractures — the doctor gently checks each joint’s position and movement to map all stiff areas. PMC

2. Craniofacial exam — measures mouth opening, jaw size, palate shape, and tongue position to gauge feeding/airway risk. Genetic Rare Disease Center

3. Neurologic exam — assesses reflexes, tone, alertness, and seizure-like events to look for brain/nerve problems. PMC

4. Airway and breathing assessment — watches breathing effort, oxygen levels, and signs of airway blockage (important if Pierre-Robin is present). Genetic Rare Disease Center

5. Growth and nutrition check — weight, length, head size, and feeding safety are reviewed to plan support. Genetic Rare Disease Center

B) Manual/functional tests

6. Goniometry of joints — a simple tool measures exact angles to document stiffness and track change over time. PMC

7. Oral-motor feeding assessment — speech/feeding therapists test suck/swallow coordination at the bedside. Genetic Rare Disease Center

8. Positioning and splint tolerance trials — therapists test gentle stretches and soft splints to see what helps without harm. PMC

9. Functional mobility screen (later infancy) — checks head control, rolling, and sitting to guide therapy goals. PMC

10. Pain and comfort scoring — ensures stretching and handling are safe and humane for the infant. (Standard neonatal care practice in AMC.) PMC

C) Laboratory and pathological tests

11. Serum creatine kinase (CK) — looks for muscle breakdown; normal CK points away from some myopathies. PMC

12. Metabolic screening panel — basic tests for treatable metabolic causes of weak movement. PMC

13. Genetic testing — chromosomal microarray and/or exome/panels for FADS/AMC genes (e.g., RAPSN, DOK7, MUSK, PIEZO2, TGFBR1, and others). Finding a variant can confirm the pathway and help family counseling. Nature+2Rare Diseases +2

14. Infection testing (TORCH, etc.) — rules out intrauterine infections that can injure brain or muscle. PMC

15. Muscle biopsy (rarely, if safe and needed) — microscopic study may show a congenital myopathy pattern. PMC

D) Electrodiagnostic tests

16. EEG — checks brain waves if jerks or seizures are suspected. Genetic Rare Disease Center

17. ECG and possible Holter monitor — looks for slow heart rhythm (bradycardia) or other rhythm issues linked to autonomic problems. Genetic Rare Disease Center

18. EMG/Nerve conduction (when feasible and ethically appropriate) — helps separate nerve vs muscle vs neuromuscular-junction causes of poor movement. PMC

E) Imaging tests

19. Prenatal ultrasound review (and fetal movement history) — very low fetal movement supports a fetal akinesia pathway. IJRCog

20. MRI/CT (postnatal as indicated) — brain MRI may show abnormalities; skeletal survey images chart contractures; swallow study (videofluoroscopy) checks if liquids enter the airway. These inform safety and care plans. autopsyandcasereports.org

Non-pharmacological treatments

1. Neonatal intensive care & airway positioning
   Purpose: keep breathing safe and stable. Mechanism: gentle positioning, continuous monitoring, oxygen/CPAP if needed. Genetic Rare Disease Center

2. Feeding therapy (speech-language/OT) with safe-swallow strategies
   Purpose: reduce choking, improve nutrition. Mechanism: thickened feeds, paced bottle, specialized nipples, and swallow training. Genetic Rare Disease Center

3. Early physical therapy
   Purpose: preserve movement and comfort. Mechanism: gentle, frequent range-of-motion and stretching to prevent worsening contractures. Cleveland Clinic

4. Occupational therapy & splinting
   Purpose: support function in hands/feet. Mechanism: custom soft splints and serial stretching to gradually improve joint position. JPOSNA

5. Serial casting for feet/hands
   Purpose: correct deformities like clubfoot. Mechanism: staged casts gradually lengthen and realign soft tissues. JPOSNA

6. Respiratory therapy & secretion management
   Purpose: prevent airway blockage and infections. Mechanism: airway suctioning, humidified air, chest physiotherapy. Genetic Rare Disease Center

7. Temperature control
   Purpose: reduce stress from dysautonomia. Mechanism: incubator/skin-to-skin with close monitoring of temperature. Genetic Rare Disease Center

8. Positioning and pressure-relief care
   Purpose: protect skin and comfort. Mechanism: frequent repositioning, cushions to avoid pressure areas. PMC

9. Orthoses (AFOs/hand splints)
   Purpose: support alignment, prevent contracture rebound. Mechanism: maintain corrected position after therapy/casting. JPOSNA

10. Hydrotherapy (gentle water-based movement)
    Purpose: reduce stiffness; safe gentle motion. Mechanism: buoyancy unloads joints and permits easier movement. JPOSNA

11. Oral-motor therapy for microstomia
    Purpose: improve mouth opening and feeding. Mechanism: graded stretching, massage, and desensitization. Genetic Rare Disease Center

12. Lactation and nutrition support
    Purpose: safe growth with high-risk feeding. Mechanism: tailored plans (breast milk or appropriate formula), calorie fortification if needed. Genetic Rare Disease Center

13. Caregiver training & home-safety teaching
    Purpose: empower parents; prevent aspiration. Mechanism: hands-on coaching for positioning, suctioning, and alarms. PMC

14. Developmental stimulation (low-stress)
    Purpose: support bonding, sensory input. Mechanism: age-appropriate, gentle, cue-based interaction. PMC

15. Palliative care integration
    Purpose: match care to family goals; maximize comfort. Mechanism: symptom-focused, team-based planning from birth. Genetic Rare Disease Center

16. Infection prevention
    Purpose: avoid pneumonia and sepsis. Mechanism: hand hygiene, oral care, suction protocols, timely vaccines per schedule. Genetic Rare Disease Center

17. Dental/oral hygiene support
    Purpose: reduce mouth infections with microstomia. Mechanism: gentle oral cleaning, moisture care. Genetic Rare Disease Center

18. Safe transport & positioning devices
    Purpose: protect airway and joints outside hospital. Mechanism: customized seats and supports. JPOSNA

19. Social work & psychosocial support
    Purpose: reduce caregiver stress; coordinate services. Mechanism: counseling, connections to rare-disease networks. Cleveland Clinic

20. Genetic counseling (for the family)
    Purpose: explain fetal-akinesia spectrum and future pregnancy considerations. Mechanism: review known/unknown causes and prenatal options. PubMed

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Drug treatments

Important safety note: There is no disease-modifying medicine for Illum syndrome. Drugs are used only to treat symptoms/complications (airway, secretions, reflux, seizures, infections, pain). Neonatal dosing is highly specialized—these examples illustrate commonly used classes, not prescriptions. Always defer to a neonatologist. Genetic Rare Disease Center

1. Oxygen/CPAP adjuncts (not a drug but paired with meds) – supports breathing during distress; reduces work of breathing. Genetic Rare Disease Center

2. Antisecretory anticholinergics (e.g., glycopyrrolate) – reduce drooling/aspiration risk by blocking muscarinic receptors in salivary glands; pediatric specialists adjust micro-doses. Genetic Rare Disease Center

3. Botulinum toxin injections to salivary glands (specialist use) – temporarily decrease saliva production to help airway safety in severe sialorrhea. Genetic Rare Disease Center

4. Proton-pump inhibitors / H2 blockers – treat reflux that worsens aspiration; decrease gastric acid secretion and esophageal irritation. Genetic Rare Disease Center

5. Prokinetics (specialist-selected) – improve gastric emptying in reflux/aspiration risk; careful risk–benefit in neonates. Genetic Rare Disease Center

6. Thickening agents (prescribed, not OTC improvisation) – reduce aspiration by slowing flow; used under feeding-team guidance. Genetic Rare Disease Center

7. Bronchodilators (if bronchospasm) – relax airway smooth muscle to ease breathing in reactive airways. Genetic Rare Disease Center

8. Mucolytics / hypertonic saline nebulization – thin secretions to clear airways; used with suction and physiotherapy. Genetic Rare Disease Center

9. Antibiotics (when infection is proven/suspected) – treat aspiration pneumonia or other infections; culture-guided. Genetic Rare Disease Center

10. Anticonvulsants (e.g., levetiracetam) – control myoclonic seizures/epileptic fits; mechanism: stabilize neuronal firing; dosing individualized. Genetic Rare Disease Center

11. Analgesia (acetaminophen; peri-operative agents) – manage pain from procedures/surgeries; careful dosing to avoid toxicity. Genetic Rare Disease Center

12. Laxatives/softeners (when needed) – prevent constipation from immobility or meds; improve comfort and feeding tolerance. Genetic Rare Disease Center

13. Antipyretics – help with fever that worsens metabolic stress; used under guidance. Genetic Rare Disease Center

14. Anticholinergic eye drops (only if ophthalmology indicates) – manage specific ocular issues like excessive tearing; specialist-guided. EyeWiki

15. Saliva substitutes / oral moisturizing gels – comfort care for microstomia and mouth dryness; protect mucosa. Genetic Rare Disease Center

16. Vitamin D and iron (if documented deficiency) – correct deficiencies that impair growth; strictly monitored in infants. Cleveland Clinic

17. Antireflux alginates (selected settings) – physical barrier to reduce reflux episodes; adjunct to positioning/feeding strategies. Genetic Rare Disease Center

18. Antiemetics (specialist-chosen if severe vomiting) – reduce vomiting that complicates feeding and aspiration risk. Genetic Rare Disease Center

19. Anticholinergic patches (older children only, specialist-led) – alternative for sialorrhea in later survivors; not for fragile neonates. Genetic Rare Disease Center

20. Peri-anesthetic precautions (malignant hyperthermia risk is discussed in related myopathic syndromes) – not a drug per se, but anesthesia teams avoid triggering agents and use meticulous airway plans when surgery is needed. Wikipedia

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Dietary molecular supplements

Because Illum syndrome affects newborns, supplements are not routine and can be unsafe without specialist oversight. When a clinician documents a need, the items below may be considered within clinical protocols. Cleveland Clinic

1. Human milk / donor milk fortifier – adds protein and calories when growth is poor; mechanism: increases nutrient density. Cleveland Clinic

2. Medium-chain triglyceride (MCT) oil (prescribed) – raises calories with smaller volumes; mechanism: easy fat absorption. Cleveland Clinic

3. Multivitamin drops for infants – address general micronutrient needs when intake is limited; mechanism: corrects potential deficits. Cleveland Clinic

4. Vitamin D – bone health and immune support as per infant guidelines; mechanism: calcium/phosphate regulation. Cleveland Clinic

5. Iron – only if deficiency or anemia; mechanism: hemoglobin synthesis. Cleveland Clinic

6. Electrolyte-balanced oral rehydration (for illness) – supports hydration when feeds are marginal; mechanism: glucose-sodium co-transport. Cleveland Clinic

7. Omega-3 enriched formula (when age-appropriate) – supports neurodevelopment; mechanism: DHA/ARA provision. Cleveland Clinic

8. Thickening systems (clinical use only) – safer swallowing; mechanism: slows liquid flow to reduce aspiration. Genetic Rare Disease Center

9. Probiotic strains (only with specialist okay) – may reduce some GI issues; mechanism: gut flora modulation—evidence in neonates is mixed. Cleveland Clinic

10. Electrolyte/trace element supplementation (IV/enteral in NICU) – corrects measured deficits during critical care. Cleveland Clinic

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Immunity-booster / regenerative / stem-cell” drugs

There are no proven immune boosters, regenerative drugs, or stem-cell therapies for Illum syndrome. Using such products outside trials can be harmful. What helps immunity safely are routine infant vaccinations, good nutrition, infection prevention, and prompt treatment of illness. Any therapy marketed as “stem-cell” for this condition should be considered unproven. Genetic Rare Disease Center

• 1) Vaccinations as scheduled – mechanism: induce protective antibodies safely. Genetic Rare Disease Center

• 2) Vitamin D if deficient – supports general health; not an “immune booster” but important. Cleveland Clinic

• 3) Nutrition optimization – human milk/fortified feeds improve resilience. Cleveland Clinic

• 4) Infection control practices – hygiene and suction protocols reduce exposure. Genetic Rare Disease Center

• 5) Prompt antibiotics for documented infection – targeted treatment, not boosting. Genetic Rare Disease Center

• 6) Palliative-care–guided symptom control – protects comfort and reduces stress burden. Genetic Rare Disease Center

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Surgeries

1. Tracheostomy – creates a stable airway when upper airway obstruction or severe secretion burden threatens life; done to secure breathing and enable long-term care. Genetic Rare Disease Center

2. Gastrostomy tube (G-tube) – provides safe nutrition when oral feeding is dangerous; done to prevent aspiration and support growth. Genetic Rare Disease Center

3. Commissuroplasty / oral releases for microstomia (highly selective) – enlarge mouth opening to improve airway access and feeding; done in carefully chosen cases by craniofacial teams. Genetic Rare Disease Center

4. Clubfoot correction (Ponseti casting ± limited releases) – correct foot position for comfort/hygiene and potential mobility; staged to minimize trauma. JPOSNA

5. Mandibular distraction (if Pierre Robin airway compromise) – moves lower jaw forward to relieve tongue-base obstruction; considered when non-surgical measures fail. Genetic Rare Disease Center

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Prevention ideas

While Illum syndrome itself cannot be reliably prevented, teams can lower risks around future pregnancies and early care: pre-pregnancy counseling, control of maternal conditions, avoid teratogens, early and repeated ultrasounds for movement checks, management of oligohydramnios when present, and delivery in a tertiary center with NICU. After birth, strict aspiration prevention, vaccination, hand hygiene, and early therapy help reduce complications. PubMed+1

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When to see a doctor

Families should seek urgent care for breathing difficulty, blue color, poor feeding or choking, lethargy, fever, stiffness that suddenly worsens, seizure-like jerks, signs of dehydration, or no wet diapers. Regular follow-up with neonatology, neurology, craniofacial/ENT, orthopedics, pulmonology, nutrition, PT/OT/SLP, and palliative care is recommended. Genetic Rare Disease Center

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What to eat / what to avoid

Eat/Use: breast milk or appropriate formula; special nipples and thickened feeds if prescribed; small, frequent feeds; careful upright positioning; and fortification if needed for growth. Avoid: unapproved thickening hacks, over-the-counter supplements, and any forced oral feeding when swallowing is unsafe—these raise the risk of aspiration. Nutrition choices must be team-directed in this condition. Genetic Rare Disease Center+1

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Frequently Asked Questions

1. Is Illum syndrome the same as Freeman-Sheldon?
   No. They share a “whistling face,” but Illum is a severe, often lethal neonatal form linked to fetal akinesia; Freeman-Sheldon (Freeman-Burian) is DA2A with MYH3 involvement and typically longer survival. Genetic Rare Disease Center+1

2. What causes Illum syndrome?
   A single cause is unknown; it fits the fetal akinesia pathway (neuromuscular problems, uterine constraint, oligohydramnios, etc.). PubMed

3. Can genetic tests help?
   They can find underlying akinesia causes in some families but may be negative in Illum syndrome itself. Nature

4. Is there a cure?
   No. Care focuses on airway, feeding, comfort, and preventing complications. Genetic Rare Disease Center

5. Do babies always die early?
   Unfortunately many do, but each case is unique. Teams tailor care to family goals and the infant’s condition. Genetic Rare Disease Center

6. Can therapy loosen joints?
   Gentle, regular therapy helps prevent worsening but cannot reverse severe congenital contractures. Cleveland Clinic

7. Is surgery safe?
   Surgery is selective and planned by experienced teams; airway and anesthesia need special precautions. Wikipedia

8. Are stem-cell treatments available?
   No proven stem-cell or “regenerative” therapies exist for Illum syndrome. Genetic Rare Disease Center

9. What about feeding tubes?
   G-tubes can safely deliver nutrition when swallowing is unsafe. Genetic Rare Disease Center

10. Can medications help drooling and choking?
    Yes—glycopyrrolate, botulinum to salivary glands, and careful feeding strategies may help selected infants. Genetic Rare Disease Center

11. Why is temperature unstable?
    The autonomic nervous system can be affected in this syndrome. Supportive thermal care helps. Genetic Rare Disease Center

12. Are vaccines safe?
    Yes—standard infant vaccines are recommended unless a specialist says otherwise. Genetic Rare Disease Center

13. How is pain managed?
    With careful neonatal dosing of analgesics and non-drug comfort strategies. Genetic Rare Disease Center

14. Can future pregnancies be checked early?
    Early, targeted ultrasounds can monitor fetal movement and anatomy; genetic counseling is advised. PubMed

15. Where can families find support?
    Rare-disease networks and multidisciplinary clinics for arthrogryposis and craniofacial conditions can help. Cleveland Clinic

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: September 23, 2025.

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