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一名患有先天性小头畸形、肌张力减退、发育迟缓、斜视、高钠血症、高镁血症和耳聋的女孩中inv(7)(q11.2q32)和del(8)(p23.1)的并发情况。

Concurrence of inv(7)(q11.2q32) and del(8)(p23.1) in a girl with congenital microcephaly, hypotonia, developmental delay, strabismus, hypernatremia, hypermagnesemia and deafness.

作者信息

Mahjoubi F, Nasiri F, Razazian F

机构信息

Cytogenetic Dept., Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran.

出版信息

Genet Couns. 2012;23(3):397-404.

Abstract

The clinical manifestations and cytogenetic details of a de novo partial deletion of the short arm of chromosome 8, del(8)(p23.1), and inversion of long arm chromosome 7, inv(7)(q11.2q32), are described. The case was a 22 month old girl referred to our cytogenetic laboratory due to many abnormal features such as congenital microcephaly, hypotonia, developmental delay, strabismus, highly arched palate, hypernatremia, hypermagnesemia and deafness. Chromosome analysis revealed 46,XX, inv(7)(q11.2q32),del(8)(p23.1) de novo karyotype. The concurrence of these two abnormalities has not been reported previously.

摘要

本文描述了一例8号染色体短臂新发部分缺失del(8)(p23.1)和7号染色体长臂倒位inv(7)(q11.2q32)的临床表现及细胞遗传学细节。该病例为一名22个月大的女童,因先天性小头畸形、肌张力减退、发育迟缓、斜视、高拱腭、高钠血症、高镁血症和耳聋等多种异常特征转诊至我们的细胞遗传学实验室。染色体分析显示核型为46,XX, inv(7)(q11.2q32),del(8)(p23.1) 新发。此前尚未有这两种异常同时出现的报道。

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