- Source: Corneodermatoosseous syndrome
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.
See also
Palmoplantar keratoderma
Keratoderma
Skin lesion
Terminal osseous dysplasia with pigmentary defects
List of cutaneous conditions