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临床试验/NCT02175264
NCT02175264已完成不适用

Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 73 人开始时间: 2014年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
73
试验地点
1
主要终点
genes responsible for isolated CDH

研究概览

简要总结

In isolated congenital diaphragmatic hernia (CDH), recurrent risk is low suggesting the occurrence of novo mutations (dominant or recessive). Our objective is to test this hypothesis by combining the search for pathogenic genomic alteration and intragenic mutations through whole exome sequencing in a homogenous group of patients.

详细描述

To elucidate the genetic basis of non syndromic congenital diaphragmatic hernia in a sub group of individuals with similar phenotype: Isolated CDH presenting with postero-lateral-left diaphragmatic defect with good perinatal outcome (n=16) To establish the prevalence of the identified gene(s) in a cohort of identical patients (n=30)

Two complementary approaches will be used:

  • Search for pathogenic genomic alterations using microarrays (~2.106 markers (SNP and CNV) in 16 trios (affected child and 2 parents).
  • Sequencing of the whole exome from patient genomic DNA (n=16)
  • Selection of unknown or very rare variants according to different criteria: recessive or dominant model, prediction of their pathogenicity, filtered on genes already known in CDH or involved in diaphragmatic development and non annotated CNV or variants of new gene(s) shared by different patients.
  • Variants will be validated by Sanger sequencing (for intragenic variants) or quantitative PCR (for CNV) on CDH cases and their parents as well as their absence on 100 controls.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
3 Months 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Families with one (or more) non syndromic CDH child
  • Signed consent form

排除标准

  • Syndromic CDH or associated with a known karyotype anomaly
  • No signed consent form
  • Not affiliated to French social security

结局指标

主要结局

genes responsible for isolated CDH

时间窗: One year

次要结局

  • prevalence of new identified genes in a cohort of CDH(One year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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