BEHCETS SYNDROME - FAMILY STUDY AND THE ELUCIDATION OF A GENETIC ROLE

被引：41
作者：
BERMAN, L
TRAPPLER, B
JENKINS, T
机构：
[1] JOHANNESBURG GEN HOSP,JOHANNESBURG,SOUTH AFRICA
[2] UNIV WITWATERSRAND,SCH MED,JOHANNESBURG 2001,SOUTH AFRICA
来源：
ANNALS OF THE RHEUMATIC DISEASES | 1979年 / 38卷 / 02期
关键词：
D O I：
10.1136/ard.38.2.118
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
A family with features of the mucocutaneous ocular syndrome is described. A 4-generation study reveals that the condition has been inherited as an autosomal dominant trait with variable expressivity. psychiatric symptoms and myalgia have been prominent features peculiar to the patients reported.
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页码：118 / 121
页数：4
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