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涉及9p部分三体和Yq部分单体的不平衡易位伴神经发育迟缓。

Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays.

作者信息

Lyons Michael J, Fuller Joshua D, Montoya Maria del Carmen, DuPont Barbara R, Holden Kenton R

机构信息

Greenwood Genetic Center, Greenwood, Charleston, SC 29418, USA.

出版信息

J Child Neurol. 2013 Apr;28(4):524-6. doi: 10.1177/0883073812446309. Epub 2012 Jun 29.

Abstract

We present a 4-year-old Honduran boy with mild neurodevelopmental delays, growth delays, dysmorphic features, and small genitalia. Chromosome analysis initially revealed a single X chromosome and a marker chromosome derived from the short arm of chromosome 9 which was consistent with Turner syndrome as only 1 sex chromosome could be identified. However, on further analysis, he was found to have an unbalanced translocation involving the short arm of chromosome 9 and the long arm of the Y chromosome. The translocation resulted in partial trisomy 9p and partial monosomy Yq. The patient's clinical features are felt to be the result of partial trisomy 9p. In addition, partial monosomy Yq is associated with male infertility. Testing of the patient's parents was normal, indicating this was a de novo translocation. Additional evaluations of this child and his parents allowed an accurate assessment of his diagnosis, long-term prognosis, and chance of recurrence.

摘要

我们报告一名4岁的洪都拉斯男孩,他有轻度神经发育迟缓、生长发育迟缓、畸形特征和小生殖器。染色体分析最初显示一条X染色体和一条源自9号染色体短臂的标记染色体,这与特纳综合征一致,因为只能识别出1条性染色体。然而,进一步分析发现,他存在涉及9号染色体短臂和Y染色体长臂的不平衡易位。这种易位导致9号染色体短臂部分三体和Y染色体长臂部分单体。患者的临床特征被认为是9号染色体短臂部分三体的结果。此外,Y染色体长臂部分单体与男性不育有关。对患者父母的检测结果正常,表明这是一次新发易位。对该患儿及其父母的进一步评估有助于准确评估其诊断、长期预后和复发几率。

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