Akbas E, Soylemez F, Hallioglu O, Polat S, Turkoz G
University of Mersin, Faculty of Medicine, Department of Medical Biology and Genetics, Mersin, Turkey.
Genet Couns. 2009;20(3):249-54.
Analysis of the SRY gene in a girl with 45,X/46,XY genotype: We present a Turner syndrome patient with a 45, X/46, XY mosaicism. A seven-year-old patient was admitted to our laboratory for evaluation of Turner Syndrome. On physical examination, short stature, a webbed neck, a broad chest with widely spaced nipples, syndactyly on toes, horse shoe kidney and typical findings of aortic coarctation were present. The chromosome karyotype of the patient was 45 X/46 XY. Molecular analysis of the blood lymphocytes confirmed the presence of the SRY gene of the patient. We report here the clinical and cytogenetic findings in a patient with an unusual sex chromosome mosaicism.
对一名具有45,X/46,XY基因型女孩的SRY基因分析:我们报告一名患有特纳综合征且具有45,X/46,XY嵌合体的患者。一名7岁患者因特纳综合征评估入住我们实验室。体格检查发现患者身材矮小、蹼颈胸廓宽阔、乳头间距宽、脚趾并指、马蹄肾以及典型的主动脉缩窄表现。患者的染色体核型为45,X/46,XY。对血液淋巴细胞的分子分析证实患者存在SRY基因。我们在此报告一名具有不寻常性染色体嵌合体患者的临床和细胞遗传学发现。