维尔纳综合征 导航菜单259.827770014096维尔纳综合征C16.320.925

糖尿病1型2型MODY1MODY 12MODY 23MODY 34MODY 45MODY 56MODY 6併發症昏迷血管病變酮酸中毒腎病變神經病變網膜病變心肌病變拉布森-門登霍爾氏綜合徵胰岛素抵抗低血糖β細胞高胰島素症G細胞左-艾二氏症侏儒症身材矮小症小矮人症萊倫氏綜合徵社會心理垂體性侏儒症巨人症自身免疫性多內分泌腺病綜合徵多發型APS1APS2類癌綜合徵多發性內分泌腺瘤12A2B早年衰老症候群维尔纳综合症肢皮早老變形性早老症伍德豪斯-沙卡第氏綜合徵腺體激素中間物代謝物礦物性皮質素生理Template:Endocrinology physiology發育Template:Development of endocrine system程序Template:Endocrine system procedures鈣平衡Template:Calcium homeostasis皮质类固醇口服降血糖藥物腦下垂體及下視丘Template:Pituitary and hypothalamic hormones and analogues甲狀腺Template:Thyroid therapy


症候群遗传病人名疾病


常染色体隐性遗传早衰症DNA螺旋酶端粒奧托·維爾納





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维尔纳综合征
Werner syndrome
分类和外部资源
醫學專科
內分泌學

ICD-9-CM

259.8
OMIM
277700
DiseasesDB
14096
Patient UK
维尔纳综合征
MeSH
C16.320.925

[编辑此条目的维基数据]

维尔纳綜合症(Werner syndrome,缩写WS)又称成人早衰症,是一种极为罕见的常染色体隐性遗传性早衰症,1904年由德国人 Otto Werner 首先报道,患者位于8号染色体短臂的、编码DNA螺旋酶的WRN基因有缺陷,患者体细胞端粒比一般人的端粒以更快的速度变短,导致在青春期后迅速衰老,出现矮身材、脱发、白发、声音嘶哑、皮肤角化、关节僵硬、肌肉萎缩、白内障等症状。目前对于该病尚无特殊治疗方法。


此病由德國醫師奧托·維爾納(Otto Werner)於1904年首先描述。



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