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3p部分三体和11q部分单体与右心室双出口及透明隔和穹窿联合部相关:一例报告

Partial trisomy 3p and partial monosomy 11q associated with double outlet right ventricle and septum pellucidum et vergae: a case report.

作者信息

Say B, Guzoglu N, Uras N, Candemir Z, Akin I, Dilmen U

机构信息

Division of Neonatology, Zekai Tahir Burak Maternity Teaching Hospital, Ankara, Turkey.

Division of Genetics, Zekai Tahir Burak Maternity Teaching Hospital, Ankara, Turkey.

出版信息

Genet Couns. 2013;24(4):387-91.

Abstract

Su Partial trisomy 3p and partial monosomy 11q are rare chromosomal disorders with a deletion of part of chromosome 11 combined with a duplication of part of chromosome 3. These are usually inherited from a parent who carries a balanced translocation involving chromosome 3, which can result in the unbalanced translocation trisomy 3p in a child. In this paper, we report a newborn who has dysmorphic facial features, double outlet right ventricle, hypotonia, hypospadias, neonatal thrombocytopenia, hydroureteronephrosis, talipes equinovarus and septum pellucidum et vergae. Cytogenetic investigation revealed 46,XY,der(11)t(3;11)(p22.2;q23.3) and the karyotype of his father showed a balanced translocation, 46XY,t(3;11)(p22.2;p23.3).

摘要

3p部分三体和11q部分单体是罕见的染色体疾病,其中11号染色体部分缺失并伴有3号染色体部分重复。这些通常遗传自携带涉及3号染色体的平衡易位的父母,这可能导致孩子出现不平衡易位三体3p。在本文中,我们报告了一名患有面部畸形、右心室双出口、肌张力低下、尿道下裂、新生儿血小板减少症、输尿管肾盂积水、马蹄内翻足和透明隔及穹窿间腔异常的新生儿。细胞遗传学检查显示为46,XY,der(11)t(3;11)(p22.2;q23.3),其父亲的核型显示为平衡易位,46XY,t(3;11)(p22.2;p23.3)。

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