Rosenthal–Kloepfer syndrome
From Wikipedia, the free encyclopedia
| Rosenthal–Kloepfer syndrome | |
|---|---|
| Classification and external resources | |
| OMIM | 102100 |
Rosenthal–Kloepfer syndrome is a cutaneous condition characterized by congenital dermatoglyph malformations.[1]
It was characterized in 1962.[2]
See also
- Amniotic band syndrome
- List of cutaneous conditions
References
- ↑ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- ↑ ROSENTHAL JW, KLOEPFER HW (December 1962). "An acromegaloid, cutis verticis gyrata, corneal leukoma syndrome. A new medical entity". Arch. Ophthalmol. 68: 722–6. PMID 13974983.
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