Cytogenetic analysis of autistic children with down syndrome features

Rajat Hegde, Smita Hegde, Pooja Joshi, Santoshkumar Gataraddi, Sujayendra Kulkarni, Gurushantappa Kadkol, S. Kulkarni, Kusal K. Das, P. Gai
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引用次数: 0

Abstract

INTRODUCTION: Autism is a heterogeneous neurodevelopmental disorder that influences a child's ability to think, learn, communicate, and interact socially and possess behavioral problems. It has also been observed to be associated with several medical conditions, including certain chromosomal disorders like Down syndrome (DS). Several studies have shown autistic individuals with DS. The main objective of the present study is to screen for chromosomal abnormalities in autistic children with DS characteristics in the North Karnataka population, India. MATERIALS AND METHODS: Chromosome analysis of peripheral blood of four DS children with autistic characteristics was performed to examine the chromosomal abnormalities, which were confirmed by fluorescent in situ hybridization. RESULTS: Childhood Autism Rating Scale score was calculated initially to assess the severity of autism. All four cases were found to have autism with DS. Out of four cases, three (75%) were found to be trisomy 21 and 1 (25%) had a trisomy 21 mosaic condition. CONCLUSION: Our study confirms the chromosomal abnormality present in autistic children with DS characteristics and these findings will contribute in several ways to the diagnosis and treatment of the genetic cause of autism with other comorbidities or vice versa.
自闭症儿童唐氏综合征特征的细胞遗传学分析
简介:自闭症是一种异质性神经发育障碍,影响儿童的思考、学习、交流和社会互动能力,并具有行为问题。它还被观察到与几种疾病有关,包括某些染色体疾病,如唐氏综合症(DS)。一些研究表明自闭症患者患有退行性痴呆。本研究的主要目的是筛查印度北卡纳塔克邦人口中具有DS特征的自闭症儿童的染色体异常。材料与方法:对4例具有自闭症特征的DS患儿外周血进行染色体分析,观察其染色体异常情况,并采用荧光原位杂交法进行证实。结果:初步计算儿童自闭症评定量表得分来评估自闭症的严重程度。所有四个病例都被发现患有自闭症伴DS。其中3例(75%)为21三体,1例(25%)为21三体镶嵌病。结论:我们的研究证实了具有DS特征的自闭症儿童存在染色体异常,这些发现将在多个方面有助于自闭症与其他合并症的遗传原因的诊断和治疗,反之亦然。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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