Annerén G, Andersson M, Page D C, Brown L G, Berg M, Läckgren G, Gustavson K H, de la Chapelle A
Department of Clinical Genetics, Akademiska Hospital, University of Uppsala, Sweden.
Am J Hum Genet. 1987 Oct;41(4):594-604.
A 2-year-old boy was found to have a 47,XXX karyotype. Restriction-fragment-length-polymorphism analysis showed that, of his three X chromosomes, one is of paternal and two are of maternal origin. The results of Y-DNA hybridization were reminiscent of those in XX males in two respects. First, hybridization to Southern transfers revealed the presence in this XXX male of sequences derived from the Y-chromosomal short arm. Second, in situ hybridization showed that this Y DNA was located on the tip of the X-chromosomal short arm. We conclude that this XXX male resulted from the coincidence of X-X nondisjunction during maternal meiosis and aberrant X-Y interchange either during or prior to paternal meiosis.
一名2岁男孩被发现核型为47,XXX。限制性片段长度多态性分析显示,他的三条X染色体中,一条来自父亲,两条来自母亲。Y-DNA杂交结果在两个方面让人联想到XX男性的情况。首先,与Southern印迹杂交显示,在这名XXX男性中存在源自Y染色体短臂的序列。其次,原位杂交表明该Y DNA位于X染色体短臂的末端。我们得出结论,这名XXX男性是由于母亲减数分裂期间X-X不分离与父亲减数分裂期间或之前异常的X-Y互换同时发生所致。