Homepage Keratoos follicularis spinulosa dekalvans psoriaasi ravi


Keratoos follicularis spinulosa dekalvans psoriaasi ravi




psoriaas guttata peanahal



Sep 8, 2003 Keratosis follicularis spinulosa decalvans (KFSD) is a rare, inherited, skin disorder that affects men predominately and is characterized by hardening of the skin (keratosis) in several parts of the body. Most frequently, the face, neck, and forearms are involved. The thickening of the skin is accompanied by the .Hum Mutat. 2010 Oct;31(10):1125-33. doi: 10.1002/humu.21335. Keratosis Follicularis Spinulosa Decalvans is caused by mutations in MBTPS2. Aten E(1), Brasz LC, Bornholdt D, Hooijkaas IB, Porteous ME, Sybert VP, Vermeer MH, Vossen RH, van der Wielen MJ, Bakker E, Breuning MH, Grzeschik KH, Oosterwijk JC, den .Jun 5, 2015 The Editor,. Sir,. Keratosis follicularis spinulosa decalvans (KFSD) is a rare X-linked disorder (1, 2) characterized by diffuse follicular hyperkeratosis, progressive scarring alopecia of scalp, eyebrows, and eyelashes and may be accompanied by photophobia, corneal and conjunctival inflammation and .CASE REPORT. Keratosis follicularis spinulosa decalvans - case report. Alceu L. C. V. BerbertI; Sônia A. O. ManteseII; Ademir RochaIII; Cláudia P. CherinIV; Carolina M. CoutoV. IAssistant Professor of the Dermatological Service of the Federal University of Uberlândia (UFU)-- Uberlândia (MG), Brazil IIAssociate Professor.Keratosis follicularis spinulosa decalvans (KFSD) is a rare X-linked disorder of keratinization of the hair follicle associated with corneal dystrophy. The clinical picture is characterized by solid follicular hyperkeratosis, especially on the exposed skin, sparse eyebrows/eyelashes, follicular scaling and scarring alopecia of the .

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