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 names | CDO syndrome[1] |
 | |
| This condition is inherited in an autosomal dominant manner | |
| Specialty | Medical genetics |
See also edit
References edit
- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Corneodermatoosseous syndrome". www.orpha.net. Retrieved 19 April 2019.
{{cite web}}: CS1 maint: numeric names: authors list (link) - ^ 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.