Haspeslagh M, Fryns J P, Holvoet M, Collen G, Dierck G, Baeke J, van den Berghe H
Centre for Human Genetics, University of Leuven, Belgium.
Clin Genet. 1991 Jun;39(6):434-41. doi: 10.1111/j.1399-0004.1991.tb03055.x.
In this study we report the results of a systematic etiological, clinical genetic study in 307 institutionalized mentally retarded adult males. Special attention is paid to the nosology of X-linked mental retardation. During the survey 63 males with one or more 'Martin Bell'-like features were identified in whom repetitive fragile Xq27-3 screenings were negative. In 13 of them, belonging to 9 different families, pedigree data were compatible with X-linked inheritance. This finding confirms the existence of one (or more) forms of fra(x) negative mental retardation with 'Martin Bell'-like features.
在本研究中,我们报告了对307名机构收容的成年男性智障患者进行的系统病因学、临床遗传学研究结果。特别关注X连锁智力迟钝的疾病分类学。在调查过程中,发现63名男性具有一个或多个类似“马丁·贝尔”的特征,其中重复性脆性Xq27 - 3筛查均为阴性。其中13人分属于9个不同家庭,系谱数据符合X连锁遗传。这一发现证实了存在一种(或多种)具有类似“马丁·贝尔”特征的脆性X阴性智力迟钝形式。