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Infantile systemic hyalinosis

Medical condition From Wikipedia, the free encyclopedia

Infantile systemic hyalinosis is an allelic autosomal-recessive condition characterized by multiple skin nodules, hyaline deposition, gingival hypertrophy, osteolytic bone lesions and joint contractures.[1]: 606 

Other namesJuvenile systemic hyalinosis
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Infantile systemic hyalinosis
Other namesJuvenile systemic hyalinosis
Infantile systemic hyalinosis is inherited in an autosomal recessive manner.
SpecialtyDermatology, medical genetics Edit this on Wikidata
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Genetics

This disease is caused by mutations in the CMG2 gene (ANTXR2).[2]

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