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
| Infantile systemic hyalinosis | |
|---|---|
| Other names | Juvenile systemic hyalinosis |
| Infantile systemic hyalinosis is inherited in an autosomal recessive manner. | |
| Specialty | Dermatology, medical genetics |