Jacobs P A, Glover T W, Mayer M, Fox P, Gerrard J W, Dunn H G, Herbst D S
Am J Med Genet. 1980;7(4):471-89. doi: 10.1002/ajmg.1320070408.
Seven families with X-linked mental retardation (MR) have been studied clinically and cytogenetically. All affected males in six of the families were found to have a fragile site on Xq in a number of their peripheral lymphocytes. The fragile site was not seen in any of the affected males in the seventh family. The affected males in the six families with the fragile X had a syndrome characterized by a variable degree of MR, macro-orchidism, a characteristic repetitive, jocular speech, normal body proportions, and large jaws and ears. The fragile X chromosome could only be detected in a proportion of female carriers and its frequency in females was found to be correlated with their mental status to be inversely correlated with their age.
对七个患有X连锁智力迟钝(MR)的家族进行了临床和细胞遗传学研究。在六个家族中,所有受影响的男性外周血淋巴细胞中均发现Xq上有一个脆性位点。在第七个家族的任何受影响男性中均未发现该脆性位点。六个具有脆性X的家族中的受影响男性患有一种综合征,其特征为不同程度的智力迟钝、巨睾症、特征性的重复性诙谐言语、正常的身体比例以及大下巴和大耳朵。脆性X染色体仅在一部分女性携带者中可检测到,且在女性中的频率与其智力状态相关,与年龄呈负相关。