Dermochondrocorneal dystrophy

Dermochondrocorneal dystrophy is characterized by osteochondrodystrophy of the hands and feet, corneal dystrophy and the presence of skin nodules clustered around the metacarpophalangeal and interphalangeal joints, around the nose and ears and on the posterior surface of the elbow. Gingival lesions may also be present. It has been described in less than 20 patients. Transmission is autosomal recessive.

Also known as: FranC'ois syndrome, François syndrome, dermochondrocorneal dystrophy, DCCD, Dermochondrocorneal dystrophy of François, Francois syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Dermochondrocorneal dystrophy itself.