Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like facies.

Abdelhafid Natiq, Siham Chafai Elalaoui, Thomas Liehr, Saïd Amzazi, Abdelaziz Sefiani
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引用次数: 1

Abstract

Chromosomal heteromorphisms are described as interindividual variation of chromosomes without phenotypic consequence. Chromosomal polymorphisms detected include most regions of heterochromatin of chromosomes 1, 9, 16 and Y and the short arms of all acrocentric chromosomes. Here, we report a girl with Down-syndrome such as facies and tremendously enlarged short arm of a chromosome 22. Fluorescence in situ hybridization (FISH) with a probe specific for all acrocentric short arms revealed that the enlargement p arms of the chromosome 22 in question contained exclusively heterochromatic material derived from an acrocentric short arm. Parental studies identified a maternal origin of this heteromorphism. Cryptic trisomy 21 of the Down-syndrome critical region was excluded by a corresponding FISH-probe. Here, we report, to the best of our knowledge, largest ever seen chromosome 22 short arm, being ~×1.5 larger than the normal long arm.

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Abstract Image

唐氏综合征样相女孩22号染色体罕见短臂异型的特征分析。
染色体异型性被描述为染色体的个体间变异而没有表型后果。检测到的染色体多态性包括染色体1、9、16和Y的大部分异染色质区域以及所有顶心染色体的短臂。在这里,我们报告一个患有唐氏综合症的女孩,如22号染色体的发育和短臂极大地扩大。荧光原位杂交(FISH)用探针特异的所有顶心短臂显示,该问题的22号染色体的扩大p臂包含来自顶心短臂的纯异色物质。亲本研究确定了这种异型性的母系起源。通过相应的fish探针排除唐氏综合征关键区域的隐性21三体。在这里,我们报告,据我们所知,最大的22号染色体短臂,比正常的长臂~×1.5大。
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