Genetic-epidemiological study of pediatric population of Krasnohrad district of Kharkiv region

O. Fedota, Y. O. Sadovnychenko, N. Movchan, O. V. Kolodiazhnyi, R. S. Dolzhenkova, L. Roshcheniuk, I. M. Kasian
{"title":"Genetic-epidemiological study of pediatric population of Krasnohrad district of Kharkiv region","authors":"O. Fedota, Y. O. Sadovnychenko, N. Movchan, O. V. Kolodiazhnyi, R. S. Dolzhenkova, L. Roshcheniuk, I. M. Kasian","doi":"10.7124/VISNYK.UTGIS.16.1.902","DOIUrl":null,"url":null,"abstract":"Aim. Study of genetic pathology burden, both monogenic and chromosomal, of pediatric population of Krasnohrad district of Kharkiv region. Methods. Epidemiological and clinical-genealogical methods have been used. The information on 252 patients aged 0– 17 years from all major sources of their registration has been analyzed. Results. The monogenic pathology burden of pediatric population was 0.28 %, chromosomal disorders burden — 0.13 %, 0.41 % in total. There were 14 nosological forms of single-gene diseases, the most common ones were sensorineural hearing loss (1:1295), congenital glaucoma (1:3884), congenital hypothyroidism (1:3884), ichthyosis (1:3884). For the past ten years there was a change in the spectrum of single-gene pathology in pediatric population of Krasnohrad district. Chromosomal abnormalities in the area were represented by Down syndrome (1:868) and Prader-Willi syndrome (1:7767). Conclusions. The genetic pathology burden of the pediatric population of the Krasnohrad district of Kharkiv region, the spectrum of monogenic and chromosomal pathology, and prevalence of their individual nosological forms are comparable to those in most European countries. Keywords: genetic pathology, prevalence, single-gene diseases, chromosomal disorders, Kharkiv region.","PeriodicalId":379244,"journal":{"name":"Visnik ukrains'kogo tovaristva genetikiv i selekcioneriv","volume":"297 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Visnik ukrains'kogo tovaristva genetikiv i selekcioneriv","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7124/VISNYK.UTGIS.16.1.902","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Aim. Study of genetic pathology burden, both monogenic and chromosomal, of pediatric population of Krasnohrad district of Kharkiv region. Methods. Epidemiological and clinical-genealogical methods have been used. The information on 252 patients aged 0– 17 years from all major sources of their registration has been analyzed. Results. The monogenic pathology burden of pediatric population was 0.28 %, chromosomal disorders burden — 0.13 %, 0.41 % in total. There were 14 nosological forms of single-gene diseases, the most common ones were sensorineural hearing loss (1:1295), congenital glaucoma (1:3884), congenital hypothyroidism (1:3884), ichthyosis (1:3884). For the past ten years there was a change in the spectrum of single-gene pathology in pediatric population of Krasnohrad district. Chromosomal abnormalities in the area were represented by Down syndrome (1:868) and Prader-Willi syndrome (1:7767). Conclusions. The genetic pathology burden of the pediatric population of the Krasnohrad district of Kharkiv region, the spectrum of monogenic and chromosomal pathology, and prevalence of their individual nosological forms are comparable to those in most European countries. Keywords: genetic pathology, prevalence, single-gene diseases, chromosomal disorders, Kharkiv region.
哈尔科夫州克拉斯诺哈拉德地区儿童遗传流行病学研究
的目标。哈尔科夫地区克拉斯诺哈德地区儿童单基因和染色体遗传病理负担的研究。方法。使用了流行病学和临床家谱方法。分析了252例0 - 17岁患者的信息,这些患者来自所有主要的登记来源。结果。儿童人群单基因病理负担为0.28%,染色体疾病负担- 0.13%,合计为0.41%。单基因疾病有14种病原学类型,最常见的是感音神经性听力损失(1:12 . 95)、先天性青光眼(1:38 . 84)、先天性甲状腺功能减退(1:38 . 84)、鱼鳞病(1:38 . 84)。在过去的十年中,Krasnohrad地区儿科人群的单基因病理谱发生了变化。该地区染色体异常以唐氏综合征(1:868)和Prader-Willi综合征(1:7 7767)为代表。结论。哈尔科夫地区Krasnohrad地区儿科人口的遗传病理负担,单基因和染色体病理谱,以及他们的个体疾病形式的患病率与大多数欧洲国家相当。关键词:遗传病理学,患病率,单基因疾病,染色体疾病,哈尔科夫地区。
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
自引率
0.00%
发文量
0
×
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:604180095
Book学术官方微信
小红书