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马尔维希尔-史密斯综合征:病例报告与综述

Mulvihill-Smith syndrome: case report and review.

作者信息

Bartsch O, Tympner K D, Schwinger E, Gorlin R J

机构信息

Institut für Klinische Genetik, Universitätsklinikum Carl Gustav Carus der Technischen Universität, Dresden, Germany.

出版信息

J Med Genet. 1994 Sep;31(9):707-11. doi: 10.1136/jmg.31.9.707.

Abstract

We report a 20 year old man with short stature, microcephaly, unusual facies, numerous pigmented naevi, hypodontia, immunodeficiency, and a high pitched voice. Tympner et al had assumed that the patient had a new syndrome of "progressive combined immunodeficiency and ectomesodermal dysplasia". We show here that the condition is identical to the Mulvihill-Smith syndrome (McKusick 176690), a progeroid disorder described in four or possibly five sporadic cases to date. We describe his clinical progress up to the age of 20 years. Our patient suffered from severe viral infections, allergic rhinitis and conjunctivitis, delayed puberty, visual loss, modest achievement in high school, and reactive depression. The immunological, facioskeletal, and dental abnormalities are presented in detail.

摘要

我们报告一名20岁男性,身材矮小、小头畸形、面容异常、有大量色素痣、牙齿发育不全、免疫缺陷且嗓音高亢。Tympner等人曾认为该患者患有“进行性联合免疫缺陷和外中胚层发育异常”的新综合征。我们在此表明,该病症与Mulvihill-Smith综合征(麦库西克编号176690)相同,这是一种类早衰疾病,迄今为止在四例或可能五例散发病例中有所描述。我们描述了他直至20岁的临床病程。我们的患者患有严重病毒感染、过敏性鼻炎和结膜炎、青春期延迟、视力丧失、高中成绩平平以及反应性抑郁。详细介绍了其免疫学、面部骨骼和牙齿异常情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0730/1050081/e599e513cd39/jmedgene00288-0047-a.jpg

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