Haim-Munk syndrome: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{Infobox_Disease | |||
| Name = Haim-Munk syndrome | |||
| Image = | |||
| Caption = | |||
| DiseasesDB = 31577 | |||
| ICD10 = | |||
| ICD9 = | |||
| ICDO = | |||
| OMIM = | |||
| MedlinePlus = | |||
| eMedicineSubj = | |||
| eMedicineTopic = | |||
| eMedicine_mult = | |||
| MeshID = | |||
}} | |||
{{SI}} | {{SI}} | ||
Revision as of 15:29, 6 August 2012
Haim-Munk syndrome | |
DiseasesDB | 31577 |
---|
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.