Allali J, Roche O, Monnet D, Brezin A, Renard G, Dufier J-L
Service d'Ophtalmologie Groupe Hospitalier Necker-Enfants Malades, Paris.
J Fr Ophtalmol. 2007 May;30(5):525-8. doi: 10.1016/s0181-5512(07)89634-3.
Anhidrotic ectodermal dysplasia is a congenital, generally X-linked dermatosis that associates facial dysmorphy, short stature, and severe blepharitis. The anomalies of the skin are epidermic abnormalities; reduction of the glands of the derm, particularly the sweat glands, explaining the hypohidrosis; onychodysplasia; trichodysplasia; and abnormal dentition. The ophthalmologic manifestations are palpebral anomalies with a reduction in or an absence of Meibomian glands, dysfunction of the Moll and Zeis glands, leading to chronic squamous blepharitis and lacrimal punctal atresia. These anomalies result in severe attacks of the ocular surface, developing during the second decade, which are often invalidating and require a rigorous follow-up to avoid corneal complications.
无汗性外胚层发育不良是一种先天性皮肤病,通常为X连锁遗传,伴有面部畸形、身材矮小和严重睑缘炎。皮肤异常包括表皮异常;真皮层腺体减少,尤其是汗腺,导致少汗;甲发育异常;毛发发育异常;以及牙齿异常。眼科表现为睑部异常,睑板腺减少或缺失,Moll腺和Zeis腺功能障碍,导致慢性鳞屑性睑缘炎和泪点闭锁。这些异常导致眼表在第二个十年期间出现严重发作,通常会导致功能丧失,需要严格随访以避免角膜并发症。