Haim-Munk syndrome: Difference between revisions
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==Overview== | ==Overview== | ||
'''Haim–Munk syndrome''' is a cutaneous condition caused by a mutation in the Cathepsin C gene.<ref name="isbn1-4160-2999-0">{{cite book |author=Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |pages= |isbn=1-4160-2999-0 |oclc= |doi= |accessdate=}}</ref> | '''Haim–Munk syndrome''' is a cutaneous condition caused by a mutation in the [[Cathepsin C]] gene.<ref name="isbn1-4160-2999-0">{{cite book |author=Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |pages= |isbn=1-4160-2999-0 |oclc= |doi= |accessdate=}}</ref> | ||
==Historical Perspective== | ==Historical Perspective== |
Revision as of 15:23, 6 August 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Palmoplantar keratoderma with periodontitis and arachnodactyly and acro-osteolysis
Overview
Haim–Munk syndrome is a cutaneous condition caused by a mutation in the Cathepsin C gene.[1]
Historical Perspective
It was named after Dr. Salim Haim and Dr. Munk.[2]
References
- ↑ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- ↑ Al Aboud K, Al Aboud D (2011). "Salim Haim and the syndrome that bears his name". Dermatology Online Journal. 17 (8): 15. PMID 21906495. Retrieved 2012-08-06.