Corneodermatoosseous syndrome
Corneodermatoosseous syndrom | |
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This condition is inherited in an autosomal dominant manner |
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.[1]
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