Corneodermatoosseous syndrome
Medical condition
| Corneodermatoosseous syndrom | |
|---|---|
| Other names | CDO syndrome[1] |
 | |
| This condition is inherited in an autosomal dominant manner | |
| Specialty | Medical genetics |
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]
See also
- Palmoplantar keratoderma
- Keratoderma
- Skin lesion
- Terminal osseous dysplasia with pigmentary defects
- List of cutaneous conditions
References
- ^ 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.
External links
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