Infantile Systemic Hyalinosis
Infantile systemic hyalinosis is an allelic autosomal-recessive condition characterized by multiple skin nodules, hyaline deposition, gingival hypertrophy, osteolytic bone lesions and joint contractures.:606
Genetics
This disease is caused by mutations in the CMG2 gene (ANTXR2).
Diagnosis
Management
See also
- Skin lesion
- List of cutaneous conditions