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通过多探针T-FISH评估,特定智力障碍患者中不存在亚端粒重排。

Absence of subtelomeric rearrangements in selected patients with mental retardation as assessed by multiprobe T FISH.

作者信息

dos Santos Suely Rodrigues, Freire-Maia Dértia Villalba

机构信息

Department of Genetics and Molecular Biology, Federal University of Rio de Janeiro State (DGBM-UNIRIO), Rio de Janeiro, RJ, Brazil.

出版信息

J Negat Results Biomed. 2012 Dec 21;11:16. doi: 10.1186/1477-5751-11-16.

DOI:10.1186/1477-5751-11-16
PMID:23259705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3546875/
Abstract

BACKGROUND

Mental retardation (MR) is a heterogeneous condition that affects 2-3% of the general population and is a public health problem in developing countries. Chromosomal abnormalities are an important cause of MR and subtelomeric rearrangements (STR) have been reported in 4-35% of individuals with idiopathic MR or an unexplained developmental delay, depending on the screening tests and patient selection criteria used. Clinical checklists such as that suggested by de Vries et al. have been used to improve the predictive value of subtelomeric screening.

FINDINGS

Fifteen patients (1-20 years old; five females and ten males) with moderate to severe MR from a genetics outpatient clinic of the Gaffrée and Guinle Teaching Hospital (HUGG) of the Federal University of Rio de Janeiro State (UNIRIO) were screened with Multiprobe T FISH after normal high resolution karyotyping. No subtelomeric rearrangements were detected even though the clinical score of the patients ranged from four to seven.

CONCLUSION

In developing countries, FISH-based techniques such as Multiprobe T FISH are still expensive. Although Multiprobe T FISH is a good tool for detecting STR, in this study it did not detect STR in patients with unexplained MR/developmental delay even though these patients had a marked chromosomal imbalance. Our findings also show that clinical scores are not reliable predictors of STR.

摘要

背景

智力迟钝(MR)是一种异质性疾病,影响着2%至3%的普通人群,在发展中国家是一个公共卫生问题。染色体异常是MR的一个重要原因,根据所使用的筛查测试和患者选择标准,在4%至35%的特发性MR或不明原因发育迟缓个体中报告了亚端粒重排(STR)。诸如de Vries等人建议的临床检查表已被用于提高亚端粒筛查的预测价值。

研究结果

对来自里约热内卢州联邦大学(UNIRIO)加夫雷和吉内尔教学医院(HUGG)遗传门诊的15名年龄在1至20岁之间(5名女性和10名男性)的中度至重度MR患者进行了正常高分辨率核型分析后,采用多探针T FISH进行筛查。尽管患者的临床评分在4至7分之间,但未检测到亚端粒重排。

结论

在发展中国家,基于FISH的技术如多探针T FISH仍然昂贵。尽管多探针T FISH是检测STR的良好工具,但在本研究中,它未在不明原因MR/发育迟缓患者中检测到STR,即使这些患者存在明显的染色体不平衡。我们的研究结果还表明,临床评分不是STR的可靠预测指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/468d/3546875/5c6ead374770/1477-5751-11-16-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/468d/3546875/c96e51c34d79/1477-5751-11-16-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/468d/3546875/5c6ead374770/1477-5751-11-16-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/468d/3546875/c96e51c34d79/1477-5751-11-16-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/468d/3546875/5c6ead374770/1477-5751-11-16-2.jpg

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2
Subtelomeric chromosome rearrangements in children with idiopathic mental retardation: applicability of three molecular-cytogenetic methods.特发性智力障碍儿童的亚端粒染色体重排:三种分子细胞遗传学方法的适用性
Croat Med J. 2006 Dec;47(6):841-50.
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Identifying infants and young children with developmental disorders in the medical home: an algorithm for developmental surveillance and screening.
在医疗之家识别发育障碍的婴幼儿:发育监测与筛查算法
Pediatrics. 2006 Jul;118(1):405-20. doi: 10.1542/peds.2006-1231.
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Clinical genetic evaluation of the child with mental retardation or developmental delays.对智力迟钝或发育迟缓儿童的临床基因评估。
Pediatrics. 2006 Jun;117(6):2304-16. doi: 10.1542/peds.2006-1006.
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