Lindgren V, Chen C P, Bryke C R, Lichter P, Page D C, Yang-Feng T L
Department of Genetics, Yale University, New Haven, CT 06510.
Hum Genet. 1992 Feb;88(4):393-8. doi: 10.1007/BF00215672.
Cytogenetic and molecular techniques were employed to determine the origin of marker chromosomes in five patients with mosaic 45,X karyotypes. The markers were shown to be derived from the X chromosome in three female patients and from the Y chromosome in one female and one male. One of the female patients, with a very small, X-derived ring chromosome, had additional phenotypic abnormalities not typically associated with Turner syndrome. In this patient, both the ring and the normal X chromosomes replicated early; perhaps the unusual phenotype is the result of both chromosomes remaining transcriptionally active. These studies illustrate the power of resolution and utility of combined cytogenetic and molecular approaches to some clinical cases.
采用细胞遗传学和分子技术来确定五名具有嵌合45,X核型患者中标记染色体的起源。结果显示,三名女性患者的标记染色体源自X染色体,一名女性和一名男性患者的标记染色体源自Y染色体。其中一名女性患者有一条非常小的、源自X染色体的环状染色体,还有一些通常与特纳综合征无关的额外表型异常。在该患者中,环状染色体和正常X染色体均早期复制;也许这种异常表型是两条染色体均保持转录活性的结果。这些研究说明了联合细胞遗传学和分子方法在某些临床病例中的分辨能力和实用性。