New Chromosomal ins(6;7)(Q13:P22) Anomaly in Klinefelter Syndrome Detected Coincidentally in Patient with Signs of Primary Hypogonadism

?mercanTopalo?lu; BahriEvren; EmineYa?ar; ?brahim?ahin

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New Chromosomal ins(6;7)(Q13:P22) Anomaly in Klinefelter Syndrome Detected Coincidentally in Patient with Signs of Primary Hypogonadism

机译：在原发性性腺功能减退症患者中偶然发现Klinefelter综合征的新染色体ins（6; 7）（Q13：P22）异常

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We described our case to show that different genetic disorders can accompany Klinefelter syndrome.

机译：我们描述了我们的病例，以表明不同的遗传疾病可伴有Klinefelter综合征。

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《Journal of Clinical Research in Pediatric Endocrinology》 |2017年第1期|共1页
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?mercanTopalo?lu; BahriEvren; EmineYa?ar; ?brahim?ahin;
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中图分类儿科学;
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1. Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delay. [J] . Weimer J, Metzke Heidemann S, Plendl H, American journal of medical genetics, Part A . 2006,第5期

机译：具有Klinefelter综合征，轻度面部异常和严重言语延迟症状的患者中两条多余的标记染色体的特征。
2. Outcome of microdissection testicular sperm extraction in azoospermic patients with Klinefelter syndrome and other sex-chromosomal anomalies [J] . AndoM., YamaguchiK., ChibaK., Systems biology in reproductive medicine . 2013,第4期

机译：无线精症患者克氏综合征及其他性染色体异常的显微解剖睾丸精子提取结果
3. Perspectives in Pediatric Pathology, Chapter 16. Klinefelter Syndrome and Other Anomalies in X and Y Chromosomes. Clinical and Pathological Entities [J] . Nistal Manuel, Paniagua Ricardo, Gonzalez-Peramato Pilar, Pediatric and developmental pathology: the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society . 2016,第4期

机译：儿科病理学的观点，第16章。X和Y染色体的Klinefelter综合征和其他异常。临床和病理学实体
4. Failure to Detect Chlamydia pneumoniae by Polymerase Chain Reaction in Patients with Acute Coronary Syndromes [C] . I. Burazor, A. Vojdani, M. Burazor, International Congress on Coronary Artery Disease . 2007

机译：急性冠状动脉综合征患者的聚合酶链反应未能检测衣原体肺炎
5. Sex Chromosomes and Testosterone: A Novel Mouse Model Sheds Light on the Etiology of Klinefelter Syndrome. [D] . Williams-Burris, Shayna Marie. 2016

机译：性染色体和睾丸激素：一种新型小鼠模型揭示了克氏综合征的病因。
6. Primary myelodysplastic syndrome with complex chromosomal rearrangements in a patient with Klinefelters syndrome. [O] . S M Abidi, M Griffiths, D G Oscier, 1986

机译：Klinefelter综合征患者的原发性骨髓增生异常综合征伴复杂的染色体重排。
7. Primary myelodysplastic syndrome with complex chromosomal rearrangements in a patient with Klinefelter's syndrome. [O] . Abidi, S M, Griffiths, M, Oscier, D G, 1986

机译：Klinefelter综合征患者的原发性骨髓增生异常综合征伴复杂的染色体重排。

New Chromosomal ins(6;7)(Q13:P22) Anomaly in Klinefelter Syndrome Detected Coincidentally in Patient with Signs of Primary Hypogonadism

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