• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肥胖症伴发发育迟缓及/或学习障碍,患者表现出其他特征:报道新的致病性拷贝数变异。

Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: report of novel pathogenic copy number variants.

机构信息

Human Genome and Stem Cell Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of Sao Paulo, Sao Paulo, Brazil.

出版信息

Am J Med Genet A. 2013 Mar;161A(3):479-86. doi: 10.1002/ajmg.a.35761. Epub 2013 Feb 7.

DOI:10.1002/ajmg.a.35761
PMID:23401328
Abstract

Obesity is a major threat to public health worldwide, and there is now mounting evidence favoring a role for the central nervous system (CNS) in weight control. A causal relationship has been recognized in both monogenic (e.g., BDNF, TRKB, and SIM1 deficiencies) and syndromic forms of obesity [e.g., Prader-Willi syndrome (PWS)]. Syndromic obesity arising from chromosomal abnormalities, that typically also affect learning and development, are often associated with congenital malformations and behavioral characteristics. We report on nine unrelated patients with a diagnosis of learning disability and/or developmental delay (DD) in addition to obesity that were found to have copy number variants (CNVs) by single nucleotide polymorphism array-based analysis. Each patient also had a distinct and complex phenotype, and most had hypotonia and other neuroendocrine issues, such as hyperphagia and hypogonadism. Molecular and clinical characterization of these patients enabled us to determine with confidence that the CNVs we observed were pathogenic or likely to be pathogenic. Overall, the CNVs reported here encompassed a candidate gene or region (e.g., SIM1) that has been reported in patients associating obesity and DD and/or intellectual disability (ID) and novel candidate genes and regions.

摘要

肥胖是全球公共卫生的主要威胁,越来越多的证据表明中枢神经系统(CNS)在体重控制中发挥作用。在单基因(如 BDNF、TRKB 和 SIM1 缺乏)和综合征形式的肥胖症[如普拉德-威利综合征(PWS)]中已经认识到因果关系。由于染色体异常引起的综合征性肥胖症,通常也会影响学习和发育,通常与先天性畸形和行为特征有关。我们报告了 9 名无关患者,他们除了肥胖之外还被诊断为学习障碍和/或发育迟缓(DD),通过基于单核苷酸多态性阵列的分析发现他们存在拷贝数变异(CNV)。每位患者还具有独特而复杂的表型,大多数患者存在肌张力低下和其他神经内分泌问题,如食欲过盛和性腺功能减退症。对这些患者进行分子和临床特征分析使我们有信心确定我们观察到的 CNV 是致病性的或可能致病性的。总的来说,这里报道的 CNV 包括了候选基因或区域(如 SIM1),这些基因或区域已在与肥胖和 DD 以及/或智力障碍(ID)相关的患者中报道过,也包括了新的候选基因和区域。

相似文献

1
Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: report of novel pathogenic copy number variants.肥胖症伴发发育迟缓及/或学习障碍,患者表现出其他特征:报道新的致病性拷贝数变异。
Am J Med Genet A. 2013 Mar;161A(3):479-86. doi: 10.1002/ajmg.a.35761. Epub 2013 Feb 7.
2
The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.基于阵列的比较基因组杂交技术在检测捷克智障和发育迟缓儿童拷贝数变异中的临床获益。
BMC Med Genomics. 2019 Jul 23;12(1):111. doi: 10.1186/s12920-019-0559-7.
3
Genomic study via chromosomal microarray analysis in a group of Romanian patients with obesity and developmental disability/intellectual disability.通过染色体微阵列分析对一组罗马尼亚肥胖和发育障碍/智力障碍患者进行基因组研究。
J Pediatr Endocrinol Metab. 2019 Jul 26;32(7):667-674. doi: 10.1515/jpem-2018-0439.
4
The usefulness of array comparative genomic hybridization in clinical diagnostics of intellectual disability in children.阵列比较基因组杂交技术在儿童智力残疾临床诊断中的应用价值。
Dev Period Med. 2014 Jul-Sep;18(3):307-17.
5
Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes.在一组孤立性和综合征性发育迟缓/智力障碍的队列中进行拷贝数变异分析,揭示了新的基因组疾病、位置效应和候选疾病基因。
Clin Genet. 2017 Oct;92(4):415-422. doi: 10.1111/cge.13009. Epub 2017 Jul 25.
6
SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.单核苷酸多态性阵列:比较四种平台对发育迟缓儿童的诊断率
BMC Med Genomics. 2014 Dec 24;7:70. doi: 10.1186/s12920-014-0070-0.
7
Diagnostic yield of the chromosomal microarray analysis in turkish patients with unexplained development delay/ıntellectual disability(ID), autism spectrum disorders and/or multiple congenital anomalies and new clinical findings.在土耳其患有不明原因发育迟缓/智力障碍 (ID)、自闭症谱系障碍和/或多发性先天畸形以及新临床发现的患者中,染色体微阵列分析的诊断产量。
Mol Biol Rep. 2024 Apr 25;51(1):577. doi: 10.1007/s11033-024-09545-y.
8
A clear bias in parental origin of de novo pathogenic CNVs related to intellectual disability, developmental delay and multiple congenital anomalies.新发致病性 CNV 与智力障碍、发育迟缓及多发先天畸形相关,其亲本来源存在明显偏向性。
Sci Rep. 2017 Mar 21;7:44446. doi: 10.1038/srep44446.
9
[Value of copy number variation analysis and chromosomal karyotyping for the diagnosis of children with intellectual disability/developmental delay].[拷贝数变异分析和染色体核型分析在智力残疾/发育迟缓儿童诊断中的价值]
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Mar 10;38(3):228-231. doi: 10.3760/cma.j.cn511374-20200319-00182.
10
Single nucleotide polymorphism array analysis of 102 patients with developmental delay and/or intellectual disability from Fujian, China.对来自中国福建的102例发育迟缓或智力残疾患者进行单核苷酸多态性阵列分析。
Clin Chim Acta. 2020 Nov;510:638-643. doi: 10.1016/j.cca.2020.08.032. Epub 2020 Aug 26.

引用本文的文献

1
Rare genetic forms of obesity in childhood and adolescence, a comprehensive review of their molecular mechanisms and diagnostic approach.儿童和青少年罕见遗传性肥胖症的分子机制和诊断方法的全面综述。
Eur J Pediatr. 2023 Nov;182(11):4781-4793. doi: 10.1007/s00431-023-05159-x. Epub 2023 Aug 23.
2
Reviewed and updated Algorithm for Genetic Characterization of Syndromic Obesity Phenotypes.对综合征性肥胖表型的遗传特征分析算法进行了审核和更新。
Curr Genomics. 2022 Jul 5;23(3):147-162. doi: 10.2174/1389202923666220426093436.
3
Bardet-Biedl syndrome: Weight patterns and genetics in a rare obesity syndrome.
Bardet-Biedl 综合征:一种罕见肥胖综合征的体重模式和遗传学。
Pediatr Obes. 2021 Feb;16(2):e12703. doi: 10.1111/ijpo.12703. Epub 2020 Jul 22.
4
Early Detection and Management of Prader-Willi Syndrome in Egyptian Patients.埃及患者普拉德-威利综合征的早期检测与管理
J Pediatr Genet. 2019 Dec;8(4):179-186. doi: 10.1055/s-0039-1695042. Epub 2019 Aug 4.
5
The effect of copy number variations in chromosome 16p on body weight in patients with intellectual disability.16 号染色体上拷贝数变异对智力障碍患者体重的影响。
J Hum Genet. 2019 Mar;64(3):221-231. doi: 10.1038/s10038-018-0545-5. Epub 2018 Dec 5.
6
Chromosomal microarray analysis in the genetic evaluation of 279 patients with syndromic obesity.279例综合征性肥胖患者基因评估中的染色体微阵列分析
Mol Cytogenet. 2018 Feb 5;11:14. doi: 10.1186/s13039-018-0363-7. eCollection 2018.
7
Genetic analysis of very obese children with autism spectrum disorder.自闭症谱系障碍的非常肥胖儿童的遗传学分析。
Mol Genet Genomics. 2018 Jun;293(3):725-736. doi: 10.1007/s00438-018-1418-5. Epub 2018 Jan 11.
8
Two New Cases of 1p21.3 Deletions and an Unbalanced Translocation t(8;12) among Individuals with Syndromic Obesity.综合征性肥胖个体中两例新的1p21.3缺失病例及一例不平衡易位t(8;12)
Mol Syndromol. 2015 Jul;6(2):63-70. doi: 10.1159/000371600. Epub 2015 Jan 28.
9
6q16.3q23.3 duplication associated with Prader-Willi-like syndrome.与普拉德-威利样综合征相关的6q16.3q23.3重复
Mol Cytogenet. 2015 Jun 25;8:42. doi: 10.1186/s13039-015-0151-6. eCollection 2015.
10
Investigation of selected genomic deletions and duplications in a cohort of 338 patients presenting with syndromic obesity by multiplex ligation-dependent probe amplification using synthetic probes.使用合成探针通过多重连接依赖探针扩增技术,对338例患有综合征性肥胖的患者队列中的选定基因组缺失和重复进行研究。
Mol Cytogenet. 2014 Oct 31;7(1):75. doi: 10.1186/s13039-014-0075-6. eCollection 2014.