Open Access Articles- Top Results for Corneodermatoosseous syndrome

Corneodermatoosseous syndrome

Corneodermatoosseous syndrome
Classification and external resources
OMIM 122440
NCI Corneodermatoosseous syndrome
Patient UK Corneodermatoosseous syndrome

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


  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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