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Infantile systemic hyalinosis
Medical condition From Wikipedia, the free encyclopedia
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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
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Genetics
This disease is caused by mutations in the CMG2 gene (ANTXR2).[2]
Diagnosis
![[icon]](#/media/File:Wiki_letter_w_cropped.svg){kind=small} | This section is empty. You can help by adding to it. (October 2017) |
Management
| This section is empty. You can help by adding to it. (October 2017) |
See also
References
External links
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