Primary lymphedema: Difference between revisions
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Lymphedema tarda occurs in patient above 35 years of age | Lymphedema tarda occurs in patient above 35 years of age | ||
'''Lymphedema–distichiasis syndrome''' is a medical condition associated with the [[FOXC2]] gene.<ref name="Andrews">{{cite book |author=James, William D.; Berger, Timothy G.; et al. |title=Andrews' Diseases of the Skin: clinical Dermatology |publisher=Saunders Elsevier |location= |year=2006 |pages= |isbn=0-7216-2921-0 |oclc= |doi= |accessdate=}}</ref>{{rp|849}} | |||
==Reference== | ==Reference== | ||
{{reflist|2}} | {{reflist|2}} |
Latest revision as of 03:04, 2 August 2013
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Mugilan Poongkunran M.B.B.S [2]
Overview
Primary lymphedema is a form of lymphedema which is not directly attributable to another medical condition.
It can be divided into three forms, depending upon age of onset: congenital lymphedema, lymphedema praecox, and lymphedema tarda.[1]
It can be familial.[2]
Lymphedema tarda occurs in patient above 35 years of age
Lymphedema–distichiasis syndrome is a medical condition associated with the FOXC2 gene.[3]:849
Reference
- ↑ http://emedicine.medscape.com/article/191350-overview#showall
- ↑ Walter Siegenthaler (21 March 2007). Differential diagnosis in internal medicine: from symptom to diagnosis. Thieme. pp. 387–. ISBN 978-1-58890-551-2. Retrieved 20 May 2011.
- ↑ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.