Turner G, Daniel A, Frost M
J Pediatr. 1980 May;96(5):837-41. doi: 10.1016/s0022-3476(80)80552-x.
Twenty-three families with X-linked mental retardation were examined for the presence of a fragil site on the long arm of the X chromosome (Xq27 fra). Specific culture media were necessary to demonstrate this site. In only seven of the families was the Xq fragile site observed; in these, all of the affected males had both the fragile X and macro-orchidism. Macro-orchidism was not observed in the remaining 16 families. In the families with Xq27 fra segregating the fraes. This correlated with the age of the carrier. The 25 affected males with macro-orchidism and Xq27 fra had some minor clinical features in common: there was an increase in birth weight, high forehead, prognathism, pale irides, big ears, and an increased head circumference in infancy and childhood which did not persist into adult life. The majority of the affected individuals were moderately retarded.
对23个患有X连锁智力迟钝的家庭进行了检查,以确定X染色体长臂(Xq27 fra)上是否存在脆性位点。需要特定的培养基来显示该位点。在这些家庭中,仅7个家庭观察到了Xq脆性位点;在这些家庭中,所有受影响的男性都有脆性X和巨睾症。在其余16个家庭中未观察到巨睾症。在Xq27 fra分离fraes的家庭中。这与携带者的年龄相关。25名患有巨睾症和Xq27 fra的受影响男性有一些共同的轻微临床特征:出生体重增加、前额高、凸颌、虹膜淡、耳朵大,以及婴儿期和儿童期头围增加,但成年后未持续。大多数受影响个体为中度智力迟钝。