Infantile systemic hyalinosis is an allelic autosomal-recessive condition characterized by multiple skin nodules, hyaline deposition, gingival hypertrophy, osteolytic bone lesions and joint contractures.
This disease is caused by mutations in the CMG2 gene (ANTXR2).
List of cutaneous conditions
GeneReview/NIH/UW entry on Hyalinosis, Inherited Systemic
Li plis nan WikipediaTape yon sentòm oswa yon maladi epi li sou remèd fèy ki ta ka ede, tape yon zèb ak wè maladi ak sentòm li itilize kont.
* Tout enfòmasyon baze sou rechèch syantifik pibliye