Corneodermatoosseous syndrom | |
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Other names | CDO syndrome [1] |
This condition is inherited in an autosomal dominant manner | |
Specialty | Medical genetics |
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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