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.[2]

Corneodermatoosseous syndrom
Other namesCDO syndrome[1]
This condition is inherited in an autosomal dominant manner

See also

References
  1. RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Corneodermatoosseous syndrome". www.orpha.net. Retrieved 19 April 2019.
  2. 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.








Classification
External resources


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