医学
流行病学
身材矮小
儿科
星团(航天器)
后备箱
鼻子
糖尿病
皮肤病科
外科
内科学
内分泌学
生态学
计算机科学
生物
程序设计语言
作者
Maria Vittoria Masala,S Scapaticci,Carla Olivieri,C Pirodda,Maria Antonietta Montesu,Maria Antonietta Cuccuru,Sara Pruneddu,Cesare Danesino,D. Cerimele
出处
期刊:PubMed
日期:2007-05-05
卷期号:17 (3): 213-6
被引量:39
标识
DOI:10.1684/ejd.2007.0155
摘要
Werner syndrome (WS, MIM#277700) is a very rare autosomal recessive disorder. WS clinical signs include altered distribution of subcutaneous fat, juvenile bilateral cataracts, a mask-like face and bird-like nose, trophic ulcers of the feet, diabetes mellitus, and premature atherosclerosis. The habitus is characteristic, with short stature, stocky trunk and slender extremities. WS frequency has been roughly estimated to be 1: 100,000 in Japan and 1: 1,000,000-1: 10,000,000 outside of Japan. The only exception to the latter data can be seen in the clustering of WS in Sardinia. Since 2001, 5 new cases have been observed: 4 members of the same family and 1 sporadic case. Therefore, since 1982 the total number of cases described in North Sardinia amounts to 18: 15 are familial (11 members of the same family group) and 3 sporadic. A short clinical description of the 5 new cases is reported.
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