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梅尔克森-罗森塔尔综合征的家系研究。该疾病的一些遗传方面及文献综述。

Family study on Melkersson-Rosenthal syndrome. Some hereditary aspects of the disease and review of literature.

作者信息

Meisel-Stosiek M, Hornstein O P, Stosiek N

机构信息

Department of Dermatology, University of Erlangen-Nürnberg, West Germany.

出版信息

Acta Derm Venereol. 1990;70(3):221-6.

PMID:1972835
Abstract

The medical records of 73 unrelated patients with either complete or incomplete Melkersson-Rosenthal syndrome attending our department between 1967 and 1985 were analyzed, and 42 of them as well as 171 of their relatives were examined. Lingua plicata was seen in 10, and other features were detected in 6 of the 42 families. The limited frequency of signs characteristic for the syndrome in the relatives examined suggest a multifactorial origin including a genetic basis.

摘要

分析了1967年至1985年间在我科就诊的73例患有完全性或不完全性梅尔克森-罗森塔尔综合征的非亲缘关系患者的病历,并对其中42例患者及其171名亲属进行了检查。在42个家族中的10个家族发现有皱襞舌,在其中6个家族检测到其他特征。在所检查亲属中该综合征特征性体征的出现频率有限,提示其起源包括遗传基础在内的多因素性。

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