Catalog

Congenital cataracts - facial dysmorphism - neuropathy

No MMS code

Link to WHO Definition

Congenital cataracts - facial dysmorphism - neuropathy – http://id.who.int/icd/entity/359570451

Congenital Cataracts Facial Dysmorphism Neuropathy (CCFDN) syndrome is a complex developmental disorder of autosomal recessive inheritance. Developmental abnormalities include congenital cataracts and microcorneae, primary hypomyelination of the peripheral nervous system, impaired physical growth, delayed early motor and intellectual development, mild facial dysmorphism and hypogonadism. Para-infectious rhabdomyolysis is a serious complication.