Medicine:Corneodermatoosseous syndrome

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Corneodermatoosseous syndrom
Other namesCDO syndrome[1]
Autosomal dominant - en.svg
This condition is inherited in an autosomal dominant manner

Corneodermatosseous 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.[2]

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