Facial Hemiatrophy

Alias:
Parry-Romberg Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
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.
Related ID:
MESH:D005150

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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12
46
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Medical Symptom

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Description
HPO Frequency
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HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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