Mattei J F, Mattei M G, Aumeras C, Auger M, Giraud F
Hum Genet. 1981;59(4):281-9. doi: 10.1007/BF00295459.
The clinical and cytogenetic features of 15 families with mental retardation linked to the fragile site on the X chromosome are presented. The 15 propositi were all prepubertal, and one was a girl. Although the clinical picture varied in severity, it was sufficiently constant to suggest the diagnosis from the facial features and the encephalopathy with language retardation and disturbed behavior. Macroorchidism was not seen before puberty. The fragile X chromosome was found in seven of the nine mothers studied and in two mildly retarded sisters and has also been demonstrated in fibroblasts in eleven subjects with the abnormality.
本文介绍了15个与X染色体脆性位点相关的智力发育迟缓家族的临床和细胞遗传学特征。15名先证者均为青春期前儿童,其中1名是女孩。尽管临床表现严重程度各异,但从面部特征、伴有语言发育迟缓及行为障碍的脑病来看,其特征足够恒定,足以提示诊断。青春期前未发现巨睾症。在所研究的9名母亲中的7名、2名轻度智力发育迟缓的姐妹中发现了脆性X染色体,并且在11名有该异常的受试者的成纤维细胞中也证实了这一点。