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本文引用的文献

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2
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Am J Hum Genet. 2015 Dec 3;97(6):848-54. doi: 10.1016/j.ajhg.2015.10.010. Epub 2015 Nov 12.
3
SG-ADVISER CNV: copy-number variant annotation and interpretation.SG-ADVISER拷贝数变异:拷贝数变异注释与解读
Genet Med. 2015 Sep;17(9):714-8. doi: 10.1038/gim.2014.180. Epub 2014 Dec 18.
4
Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome.一个患有t(3;13)(q26.2;p11.2)的家族的临床、细胞遗传学和生化分析:3q重复综合征的进一步描述
Case Rep Genet. 2013;2013:895259. doi: 10.1155/2013/895259. Epub 2013 Sep 18.
5
A boy with partial trisomy of chromosome 3q24-q28 from paternal balanced insertion and multiple congenital anomalies.患儿来自父源平衡插入的 3q24-q28 部分三体,伴多发先天畸形。
Am J Med Genet A. 2013 Feb;161A(2):327-30. doi: 10.1002/ajmg.a.35637. Epub 2013 Jan 15.
6
Deletion of the 3q26 region including the EVI1 and MDS1 genes in a neonate with congenital thrombocytopenia and subsequent aplastic anaemia.3q26 区缺失包括 EVI1 和 MDS1 基因的新生儿先天性血小板减少症和随后的再生障碍性贫血。
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Ecotropic viral integration site 1, stem cell self-renewal and leukemogenesis.嗜同性病毒整合位点 1、干细胞自我更新与白血病发生。
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Prenatal diagnosis of partial trisomy 3q resulting from t(3;14) in a fetus with multiple anomalies including vermian hypoplasia.胎儿多发畸形包括蚓部发育不全,经染色体核型分析发现其存在 3;14 易位,导致部分 3q 三体,对此进行了产前诊断。
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9
Delineation of the breakpoints of pure duplication 3q due to a de novo duplication event using SOMA.使用SOMA对由于新发重复事件导致的纯3q重复的断点进行描绘。
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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.共识声明:对于患有发育障碍或先天畸形的个体,染色体微阵列是一线临床诊断测试。
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一个位于3q重复综合征关键区域近端的纯合2兆碱基3q26.2重复。

A Pure 2-Mb 3q26.2 Duplication Proximal to the Critical Region of 3q Duplication Syndrome.

作者信息

Coelho Molck Miriam, Simioni Milena, Paiva Vieira Társis, Paoli Monteiro Fabíola, Gil-da-Silva-Lopes Vera L

机构信息

Department of Medical Genetics, University of Campinas (UNICAMP), Campinas, Brazil.

出版信息

Mol Syndromol. 2018 Jul;9(4):197-204. doi: 10.1159/000489870. Epub 2018 Jun 8.

DOI:10.1159/000489870
PMID:30140197
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6103331/
Abstract

Partial duplication of chromosome 3q - dup(3q) - is a recognizable syndrome with dysmorphic facial features, microcephaly, digital anomalies, and genitourinary and cardiac defects, as well as growth retardation and developmental delay. Most cases of dup(3q) result from unbalanced translocations or inversions and are accompanied by additional chromosomal imbalances. Pure dup(3q) is rare, and only 31 cases have been reported so far. We report a new case of a girl with a pure 2-Mb duplication at 3q26.2 not encompassing the known critical region 3q26.3q27. After an extensive review, to the best of our knowledge, the case herein presented harbors the shortest 3q duplication of this region. The clinical phenotype of this patient resembles previously reported cases of pure dup(3q) syndrome, including intellectual disability, synophrys, a wide nasal bridge, dysmorphic ears, clinodactyly, and cardiac defects. We suggest that the 3q26.2 duplication is a candidate copy number alteration explaining our patient's clinical phenotype.

摘要

3号染色体长臂部分重复(dup(3q))是一种可识别的综合征,具有面部畸形、小头畸形、手指异常、泌尿生殖系统和心脏缺陷,以及生长发育迟缓。大多数dup(3q)病例是由不平衡易位或倒位引起的,并伴有其他染色体不平衡。纯合dup(3q)很少见,迄今为止仅报道了31例。我们报告了一例新病例,一名女孩在3q26.2处有一个2兆碱基的纯合重复,未涉及已知的关键区域3q26.3q27。经过广泛查阅,据我们所知,本文所呈现的病例是该区域最短的3q重复。该患者的临床表型与先前报道的纯合dup(3q)综合征病例相似,包括智力残疾、连眉、宽鼻梁、耳部畸形、手指弯曲和心脏缺陷。我们认为3q26.2重复是解释我们患者临床表型的一个候选拷贝数改变。