Infantile systemic hyalinosis is an allelic autosomal-recessive condition characterized by multiple skin nodules, hyaline deposition, gingival hypertrophy, osteolytic bone lesions and joint contractures.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .

Genetics

This disease is caused by mutations in the CMG2 gene (ANTXR2). See also Skin lesion List of cutaneous conditions

References

External links GeneReview/NIH/UW entry on Hyalinosis, Inherited Systemic