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A Case Report of Rosenthal-Kloepfer Syndrome


  • Dept. of Medicine, BJ medical college, Ahmedabad, India


Rosenthal-Kloepfer syndrome is a very rare disorder characterized by acromegaloid features, furrowed skin on scalp and face and corneal leukomas. Here we are presenting this rare syndrome in a man who presented with bilateral corneal leukoma, cutis verticis gyrate and acromegaloid features.

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  • Harbison J B, Nice C M, Jr. Familial pachydermoperiostosis presenting as an acromegaly-like syndrome. Am J Roentgen Radium Ther Nucl Med. 1971;112:532-536,
  • McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders, 12th ed. Baltimore: The Johns Hopkins University Press, 1998
  • Rosenthal, J. W, Kloepfer, H. W. An acromegaloid, cutis verticis gyrata, corneal leukoma syndrome: a new medical entity. Arch. Ophthal. 1962;68:722-726.
  • Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007).Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-41602999-0.
  • Online Mendelian Inheritance in Man, OMIM. McKusickNathans Institute for Genetic Medicine, Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine, February 12, 2007.
  • OMIM ID: 102100 Emery & Rimoin’s: Principles and Practice of Medical Genetics. Church. Livingstone. p.1916, 2007
  • Lyle WM, Williams TD. Genes in Eyecare : geneseyedoc 3. 15 Mar 04.


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