The Frequency of Consanguinity and Its Related Factors in Parents of Children with Genetic Disorders

Q3 Medicine
Sajjad Biglari, A. Biglari, S. Mazloomzadeh
{"title":"The Frequency of Consanguinity and Its Related Factors in Parents of Children with Genetic Disorders","authors":"Sajjad Biglari, A. Biglari, S. Mazloomzadeh","doi":"10.30699/jambs.30.143.501","DOIUrl":null,"url":null,"abstract":"10.30699/jambs.30.143.501 Background & Objective: Consanguinity increases the incidence of genetic disorders. The frequency of consanguinity varies in different societies. There was no data regarding the frequency of consanguinity in Zanjan province. This study aimed to describe the prevalence of consanguineous unions in the parents of children with genetic disorders and its related factors in Zanjan, Iran. Materials & Methods: This cross-sectional study included children with genetic diseases referring to the medical genetics clinic in Zanjan's Musavi Hospital during 2014-2018. Data including consanguineous unions in families (up to three previous generations), types of genetic illnesses, child and parents' age, parental educational level, and occupation were collected and analyzed using descriptive statistics, independent t-test, and chi-square test. Results: Of the 87 children, 41 (47.7%) were male, and 50 (59.5%) resided in urban areas. The mean age of the children was 6.5 years. The educational level of 56.6% of fathers and 50.6% of mothers were highschool diploma or higher. The parents of 44 children (51.8%) had consanguineous unions. The most common type of consanguineous union was between first cousins. The nature of the genetic disorders in 63 (72.4%) of children was molecular. The proportion of consanguinity was significantly higher in parents of children with molecular than chromosomal disorder (P<0.0001). Consanguinity had also a significant relationship with the children's age (P=0.04). Conclusion: This study's outcomes illustrate that parents of more than half of children with genetic disorders had consanguinity and the frequency of consanguinity was more common in parents of children with molecular disease than chromosomal disorder. Given that, it is necessary to avoid consanguineous marriage as much as possible, and families with a history of molecular genetic disease, should be informed of the possible consequences.","PeriodicalId":36550,"journal":{"name":"Journal of Advances in Medical and Biomedical Research","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Advances in Medical and Biomedical Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30699/jambs.30.143.501","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 1

Abstract

10.30699/jambs.30.143.501 Background & Objective: Consanguinity increases the incidence of genetic disorders. The frequency of consanguinity varies in different societies. There was no data regarding the frequency of consanguinity in Zanjan province. This study aimed to describe the prevalence of consanguineous unions in the parents of children with genetic disorders and its related factors in Zanjan, Iran. Materials & Methods: This cross-sectional study included children with genetic diseases referring to the medical genetics clinic in Zanjan's Musavi Hospital during 2014-2018. Data including consanguineous unions in families (up to three previous generations), types of genetic illnesses, child and parents' age, parental educational level, and occupation were collected and analyzed using descriptive statistics, independent t-test, and chi-square test. Results: Of the 87 children, 41 (47.7%) were male, and 50 (59.5%) resided in urban areas. The mean age of the children was 6.5 years. The educational level of 56.6% of fathers and 50.6% of mothers were highschool diploma or higher. The parents of 44 children (51.8%) had consanguineous unions. The most common type of consanguineous union was between first cousins. The nature of the genetic disorders in 63 (72.4%) of children was molecular. The proportion of consanguinity was significantly higher in parents of children with molecular than chromosomal disorder (P<0.0001). Consanguinity had also a significant relationship with the children's age (P=0.04). Conclusion: This study's outcomes illustrate that parents of more than half of children with genetic disorders had consanguinity and the frequency of consanguinity was more common in parents of children with molecular disease than chromosomal disorder. Given that, it is necessary to avoid consanguineous marriage as much as possible, and families with a history of molecular genetic disease, should be informed of the possible consequences.
遗传性疾病患儿父母的血亲频率及其相关因素
10.30699/jambs.30.143.501背景与目的:血缘关系会增加遗传疾病的发生率。血亲的频率在不同的社会中各不相同。没有关于赞詹省近亲交配频率的数据。本研究旨在描述伊朗赞詹遗传病儿童父母近亲结合的流行情况及其相关因素。材料与方法:这项横断面研究包括2014-2018年期间在赞詹穆萨维医院的医学遗传学诊所就诊的遗传病儿童。使用描述性统计、独立t检验和卡方检验收集和分析数据,包括家庭(最多前三代)的血缘结合、遗传疾病类型、儿童和父母的年龄、父母的教育水平和职业。结果:在87名儿童中,41名(47.7%)为男性,50名(59.5%)居住在城市地区。儿童的平均年龄为6.5岁。56.6%的父亲和50.6%的母亲的教育水平为高中以上学历。44名儿童(51.8%)的父母有血缘关系。最常见的血缘结合类型是表亲之间。63名(72.4%)儿童的遗传性疾病是分子性的。分子障碍儿童的父母的血亲比例显著高于染色体障碍儿童(P<0.0001)。血亲与儿童年龄也有显著关系(P=0.04)父母患有分子疾病的儿童比染色体疾病的儿童多。鉴于此,有必要尽可能避免近亲结婚,并应告知有分子遗传疾病史的家庭可能的后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
0.90
自引率
0.00%
发文量
94
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信