Rosenthal–Kloepfer syndrome

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

References

  1. ↑ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
  2. ↑ ROSENTHAL JW, KLOEPFER HW (December 1962). "An acromegaloid, cutis verticis gyrata, corneal leukoma syndrome. A new medical entity". Arch. Ophthalmol. 68: 722–6. doi:10.1001/archopht.1962.00960030726004. PMID 13974983.


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