Corneodermatoosseous syndrome
| Corneodermatoosseous syndrome |
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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]
See also
- Palmoplantar keratoderma
- Keratoderma
- Skin lesion
- Terminal osseous dysplasia with pigmentary defects
- List of cutaneous conditions
References
- ^ Stevens, Howard P.; David P. Kelsell, and Irene M. Leigh (2003). "Chapter 52: The Inherited Keratodermas of Palms and Soles". In Freedberg; et al. (eds.). Fitzpatrick's Dermatology in General Medicine (6th ed.). McGraw-Hill. p. 513. ISBN 0-07-138067-1.
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