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

• Palmoplantar keratoderma
• Keratoderma
• Skin lesion
• Terminal osseous dysplasia with pigmentary defects
• List of cutaneous conditions

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. pp. 513. ISBN 0-07-138067-1. 

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