Haim-Munk syndrome: Difference between revisions
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{{Infobox_Disease | |||
| Name = Haim-Munk syndrome | |||
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| DiseasesDB = 31577 | |||
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{{SI}} | {{SI}} | ||
{{CMG}} | {{CMG}} | ||
{{SK}} Palmoplantar keratoderma with periodontitis and arachnodactyly and acro-osteolysis | {{SK}} Palmoplantar keratoderma with periodontitis and arachnodactyly and acro-osteolysis; Cochin Jewish disorder | ||
==Overview== | ==Overview== | ||
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==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
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[[Category:dermatology]] | |||
Latest revision as of 15:30, 6 August 2012
| Haim-Munk syndrome | |
| DiseasesDB | 31577 |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Palmoplantar keratoderma with periodontitis and arachnodactyly and acro-osteolysis; Cochin Jewish disorder
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.