WebJun 8, 2014 · In 1964, Alezzandrini [ 2] described 3 patients with unilateral tapetoretinal degeneration of the eye associated with ipsilateral facial vitiligo and poliosis. Two of … WebFeb 2, 2024 · 转自Wikipedia。 VHL综合征的定义:希佩尔-林道综合征(Von Hippel–Lindau disease,VHL综合征)是一种罕见的常染色体显性遗传性疾病[1],表现为血管母细胞瘤累及小脑、脊髓、肾脏以及视网膜。其若干病变包括肾脏…
Alezzandrini syndrome - About the Disease - Genetic …
Web2024罕见病诊疗指南—奥尔波特综合征 Alport syndrome. 概述. 奥尔波特综合征 Alport syndrome(本文后称 Alport 综合征)是一种遗传性胶原病,为编码Ⅳ型胶原蛋白α-3 链、α-4 链和α-5 链的基因 COL4An(n=3、4、5)突变导致的基底膜病变。. 最常累及肾脏,其次累及眼和耳。. WebThe cause of Alezzandrini syndrome remains unknown. Viral or autoimmune processes leading to melanocyte destruction have been suggested. Melanocytes are located in the skin, retina, uvea, cochlea, and vestibular labyrinth, so any of these sites may be affected. Alezzandrini syndrome is probably related to Vogt-Koyanagi-Harada (VKH) syndrome, … hawaii it services
Waardenburg syndrome - Wikipedia
WebAbout Alezzandrini syndrome. Many rare diseases have limited information. Currently GARD aims to provide the following information for this disease: Population Estimate: … WebOct 15, 2016 · 知乎,中文互联网高质量的问答社区和创作者聚集的原创内容平台,于 2011 年 1 月正式上线,以「让人们更好的分享知识、经验和见解,找到自己的解答」为品牌使命。知乎凭借认真、专业、友善的社区氛围、独特的产品机制以及结构化和易获得的优质内容,聚集了中文互联网科技、商业、影视 ... WebWaardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye), a white forelock or patches of light skin. These basic features constitute type 2 of the condition; in type 1, there is also a … hawaii itt military ticket office