Corneodermatosseous syndrome
Encyclopedia
Corneodermatosseous syndrome (also known as "CDO syndrome") is an autosomal dominant condition with onset in infancy, characterized by corneal dystrophy, photophobia, diffuse palmoplantar keratoderma, distal onycholysis, skeletal abnormalities, with brachydactyly, short stature, and medullary narrowing of digits.
See also
- Palmoplantar keratodermaPalmoplantar keratodermaPalmoplantar keratodermas are a heterogeneous group of disorders characterized by abnormal thickening of the palms and soleAutosomal recessive and dominant, X-linked, and acquired forms have all been described.There are also acquired forms of the condition....
- KeratodermaKeratoderma-Congenital:* Simple keratodermas** Diffuse palmoplantar keratodermas*** Diffuse epidermolytic palmoplantar keratoderma*** Diffuse nonepidermolytic palmoplantar keratoderma*** mal de Meleda** Focal palmoplantar keratoderma*** Striate palmoplantar keratoderma...
- Skin lesion
- Terminal osseous dysplasia with pigmentary defectsTerminal osseous dysplasia with pigmentary defectsTerminal osseous dysplasia with pigmentary defects is a cutaneous condition characterized by hyperpigmented, atrophic facial macules.It has been associated with FLNA.- See also :* Corneodermatosseous syndrome* Osseous choristoma of the tongue...
- List of cutaneous conditions