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斯里兰卡接受特殊教育儿童的脆性X综合征/CGG重复序列扩增的串联筛查。

Cascade Screening for Fragile X Syndrome/CGG Repeat Expansions in Children Attending Special Education in Sri Lanka.

作者信息

Chandrasekara C H W M R Bhagya, Wijesundera W S Sulochana, Perera Hemamali N, Chong Samuel S, Rajan-Babu Indhu-Shree

机构信息

Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Colombo, Kynsey road, Colombo 08, Sri Lanka.

Department of Psychological Medicine, Faculty of Medicine, University of Colombo, Kynsey road, Colombo 08, Sri Lanka.

出版信息

PLoS One. 2015 Dec 22;10(12):e0145537. doi: 10.1371/journal.pone.0145537. eCollection 2015.

Abstract

Fragile X syndrome (FXS) is the commonest cause of inherited mental retardation and clinically presents with learning, emotional and behaviour problems. FXS is caused by expansion of cytosine-guanine-guanine (CGG) repeats present in the 5' untranslated region of the FMR1 gene. The aim of this study was to screen children attending special education institutions in Sri Lanka to estimate the prevalence of CGG repeat expansions. The study population comprised a representative national sample of 850 children (540 males, 310 females) with 5 to 18 years of age from moderate to severe mental retardation of wide ranging aetiology. Screening for CGG repeat expansion was carried out on DNA extracted from buccal cells using 3' direct triplet primed PCR followed by melting curve analysis. To identify the expanded status of screened positive samples, capillary electrophoresis, methylation specific PCR and Southern hybridization were carried out using venous blood samples. Prevalence of CGG repeat expansions was 2.2%. Further classification of the positive samples into FXS full mutation, pre-mutation and grey zone gave prevalence of 1.3%, 0.8% and 0.1% respectively. All positive cases were male. No females with FXS were detected in our study may have been due to the small sample size.

摘要

脆性X综合征(FXS)是遗传性智力迟钝最常见的病因,临床上表现为学习、情感和行为问题。FXS是由FMR1基因5'非翻译区存在的胞嘧啶-鸟嘌呤-鸟嘌呤(CGG)重复序列扩增引起的。本研究的目的是对斯里兰卡特殊教育机构的儿童进行筛查,以估计CGG重复序列扩增的患病率。研究人群包括一个具有代表性的全国样本,共850名5至18岁的儿童(540名男性,310名女性),病因广泛,患有中度至重度智力迟钝。使用3'直接三联体引物PCR从颊细胞提取的DNA上进行CGG重复序列扩增筛查,随后进行熔解曲线分析。为了确定筛查阳性样本的扩增状态,使用静脉血样本进行毛细管电泳、甲基化特异性PCR和Southern杂交。CGG重复序列扩增的患病率为2.2%。将阳性样本进一步分类为FXS全突变、前突变和灰色区域,患病率分别为1.3%、0.8%和0.1%。所有阳性病例均为男性。在我们的研究中未检测到女性FXS患者,这可能是由于样本量较小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8df/4687912/da0228ef9705/pone.0145537.g001.jpg

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