Corneodermatoosseous syndrome

Corneodermatoosseous syndrome
Classification and external resources
OMIM 122440

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

References

  1. ↑ Stevens, Howard P.; David P. Kelsell, and Irene M. Leigh (2003). "Chapter 52: The Inherited Keratodermas of Palms and Soles". In Freedberg; et al. Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. p. 513. ISBN 0-07-138067-1.


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