Sarkar R, Marimuthu K M
Clin Genet. 1983 Dec;24(6):420-8. doi: 10.1111/j.1399-0004.1983.tb00097.x.
This study, based on the investigations carried on 82 cases of Turners of which 50 of them were mosaics and 85 cases of Klinefelters of which 70 of them were mosaics, is an attempt to explain the vast range of clinical variations observed in cytogenetically established Turner mosaics (45,X/46,XX) and Klinefelter mosaics (47,XXY/46,XY) in the light of the degree of mosaicism present in them. It was observed that the severity of the syndrome in Turner mosaics and Klinefelter mosaics increased with the relative increase in the abnormal cell line population.
本研究基于对82例特纳综合征患者(其中50例为嵌合体)和85例克兰费尔特综合征患者(其中70例为嵌合体)的调查,试图根据特纳嵌合体(45,X/46,XX)和克兰费尔特嵌合体(47,XXY/46,XY)中存在的嵌合程度,来解释在细胞遗传学确诊的这些病例中观察到的广泛临床变异。研究发现,特纳嵌合体和克兰费尔特嵌合体综合征的严重程度随着异常细胞系群体的相对增加而增加。