Facial Hemiatrophy

Facial Hemiatrophy(来自ICD-11)
别称:
Parry-Romberg Syndrome
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Medical Symptom
Gene & Mutation
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Facial Hemiatrophy, also known as parry-romberg syndrome, is related to localized scleroderma and systemic scleroderma, and has symptoms including ataxia and oral manifestations. An important gene associated with Facial Hemiatrophy is FNDC10 (Fibronectin Type III Domain Containing 10). The drugs Curcumin and Narcotics have been mentioned in the context of this disorder. Affiliated tissues include skin and bone marrow.
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相关ID:
MESH:D005150

基础信息

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参考文献
MALACARDS
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Unknown
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12
46
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