Corneodermatoosseous syndrome
Corneodermatoosseous syndrom | |
---|---|
Other names | CDO syndrome[1] |
This condition is inherited in an autosomal dominant manner |
Corneodermatosseous syndrome is an
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) - ISBN 0-07-138067-1.