北印度人群口腔唇裂遗传的皮肤纹学和唇镜检查。

National journal of maxillofacial surgery Pub Date : 2025-01-01 Epub Date: 2025-04-28 DOI:10.4103/njms.njms_166_23
Merin Paul, Mridul Khanduri, Jyotsna Jha, Mahinder Singh, Taruna Puri, Varun Kashyap
{"title":"北印度人群口腔唇裂遗传的皮肤纹学和唇镜检查。","authors":"Merin Paul, Mridul Khanduri, Jyotsna Jha, Mahinder Singh, Taruna Puri, Varun Kashyap","doi":"10.4103/njms.njms_166_23","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Cleft lip and palate (CLP) is one of the most common congenital malformations occurring in the craniofacial region. Causes of CLP can be attributed to the genetics and environmental factors. Potential advantages of prenatal diagnosis of oral cleft include psycho-social preparation, opportunity for parent education, planned neonatal care, anticipation on possible feeding problems, and increased reproductive awareness. Dermatoglyphic analysis and cheiloscopic analysis are now beginning to prove themselves as an extremely useful tool for preliminary investigations into conditions with a suspected genetic basis.</p><p><strong>Materials and methods: </strong>The study consisted of two groups of 45 parents and siblings each of cleft lip with/without palate, CL (P)-affected children (group A) and normal children (group B). The study aimed to evaluate the inheritance of cleft lip and palate in North Indian patients using dermatoglyphics and cheiloscopy. Prints of all ten fingers were taken by the Ink method and recorded on white paper. Lip patterns were obtained by direct photography of the subjects in the natural head position.</p><p><strong>Results: </strong>Increased inter-digital asymmetry (with an increased score) was seen in mothers and fathers of group A. The loop pattern was seen more in the mothers, fathers, and siblings of group A. The Type O pattern was seen only in group A in only the fathers and mothers.</p><p><strong>Conclusion: </strong>A highly significant correlation was observed in finger prints and lip patterns in parents with CL (P)-affected children and hence can prove to be an extremely useful screening tool for CL(P) and other associated genetic anomalies.</p>","PeriodicalId":101444,"journal":{"name":"National journal of maxillofacial surgery","volume":"16 1","pages":"56-62"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12156860/pdf/","citationCount":"0","resultStr":"{\"title\":\"Dermatoglyphics and cheiloscopy in inheritance of oral clefts in North Indian population.\",\"authors\":\"Merin Paul, Mridul Khanduri, Jyotsna Jha, Mahinder Singh, Taruna Puri, Varun Kashyap\",\"doi\":\"10.4103/njms.njms_166_23\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Cleft lip and palate (CLP) is one of the most common congenital malformations occurring in the craniofacial region. Causes of CLP can be attributed to the genetics and environmental factors. Potential advantages of prenatal diagnosis of oral cleft include psycho-social preparation, opportunity for parent education, planned neonatal care, anticipation on possible feeding problems, and increased reproductive awareness. Dermatoglyphic analysis and cheiloscopic analysis are now beginning to prove themselves as an extremely useful tool for preliminary investigations into conditions with a suspected genetic basis.</p><p><strong>Materials and methods: </strong>The study consisted of two groups of 45 parents and siblings each of cleft lip with/without palate, CL (P)-affected children (group A) and normal children (group B). The study aimed to evaluate the inheritance of cleft lip and palate in North Indian patients using dermatoglyphics and cheiloscopy. Prints of all ten fingers were taken by the Ink method and recorded on white paper. Lip patterns were obtained by direct photography of the subjects in the natural head position.</p><p><strong>Results: </strong>Increased inter-digital asymmetry (with an increased score) was seen in mothers and fathers of group A. The loop pattern was seen more in the mothers, fathers, and siblings of group A. The Type O pattern was seen only in group A in only the fathers and mothers.</p><p><strong>Conclusion: </strong>A highly significant correlation was observed in finger prints and lip patterns in parents with CL (P)-affected children and hence can prove to be an extremely useful screening tool for CL(P) and other associated genetic anomalies.</p>\",\"PeriodicalId\":101444,\"journal\":{\"name\":\"National journal of maxillofacial surgery\",\"volume\":\"16 1\",\"pages\":\"56-62\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12156860/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"National journal of maxillofacial surgery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/njms.njms_166_23\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/4/28 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"National journal of maxillofacial surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/njms.njms_166_23","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/28 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

摘要唇腭裂(CLP)是发生在颅面区域最常见的先天性畸形之一。CLP的病因可归因于遗传和环境因素。产前诊断唇裂的潜在优势包括心理社会准备,父母教育的机会,有计划的新生儿护理,对可能的喂养问题的预测,以及提高生殖意识。皮纹分析和唇镜分析现在开始证明自己是一种非常有用的工具,用于初步调查疑似遗传基础的疾病。材料与方法:将有/无腭裂唇裂患儿(A组)和正常唇裂患儿(B组)父母及兄弟姐妹各45人分为两组。本研究旨在评估北印度唇腭裂患者的遗传,采用皮肤刻印和唇腭裂镜检。所有十个手指的指纹都用墨迹法取下,并记录在白纸上。嘴唇图案是通过直接拍摄受试者的自然头部位置获得的。结果:A组的母亲和父亲的手指间不对称性增加(得分增加),A组的母亲、父亲和兄弟姐妹的环路模式更多,O型模式只在A组的父亲和母亲中出现。结论:在患有CL(P)的儿童中,父母的指纹和唇型具有高度显著的相关性,因此可以证明是CL(P)和其他相关遗传异常的非常有用的筛查工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dermatoglyphics and cheiloscopy in inheritance of oral clefts in North Indian population.

Dermatoglyphics and cheiloscopy in inheritance of oral clefts in North Indian population.

Dermatoglyphics and cheiloscopy in inheritance of oral clefts in North Indian population.

Dermatoglyphics and cheiloscopy in inheritance of oral clefts in North Indian population.

Introduction: Cleft lip and palate (CLP) is one of the most common congenital malformations occurring in the craniofacial region. Causes of CLP can be attributed to the genetics and environmental factors. Potential advantages of prenatal diagnosis of oral cleft include psycho-social preparation, opportunity for parent education, planned neonatal care, anticipation on possible feeding problems, and increased reproductive awareness. Dermatoglyphic analysis and cheiloscopic analysis are now beginning to prove themselves as an extremely useful tool for preliminary investigations into conditions with a suspected genetic basis.

Materials and methods: The study consisted of two groups of 45 parents and siblings each of cleft lip with/without palate, CL (P)-affected children (group A) and normal children (group B). The study aimed to evaluate the inheritance of cleft lip and palate in North Indian patients using dermatoglyphics and cheiloscopy. Prints of all ten fingers were taken by the Ink method and recorded on white paper. Lip patterns were obtained by direct photography of the subjects in the natural head position.

Results: Increased inter-digital asymmetry (with an increased score) was seen in mothers and fathers of group A. The loop pattern was seen more in the mothers, fathers, and siblings of group A. The Type O pattern was seen only in group A in only the fathers and mothers.

Conclusion: A highly significant correlation was observed in finger prints and lip patterns in parents with CL (P)-affected children and hence can prove to be an extremely useful screening tool for CL(P) and other associated genetic anomalies.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
1.20
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