Zobrazeno 1 - 10
of 2 129
pro vyhledávání: '"OROFACIAL CLEFTS"'
Publikováno v:
International Dental Journal, Vol 74, Iss 6, Pp 1413-1423 (2024)
ABSTRACT: Objectives: Metabolic syndrome (MetS) has been suggested to play a role in congenital defects. This study investigated the association of MetS and its components with orofacial clefts (OFCs). Methods: We conducted a case-control study in No
Externí odkaz:
https://doaj.org/article/07eaa377cf814beea7d757a7635482e2
Publikováno v:
BMC Oral Health, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background The epidemiology of cleft lip (CL) and cleft palate (CLP) has not previously been described in the context of the Bhutan and Bhutanese populations. Using National Birth Defects Surveillance Data and other vital statistics, we pres
Externí odkaz:
https://doaj.org/article/8faaf1c2b2d140c8ad22b36fe19b1124
Autor:
Mishal Muhammed Haris, J Dimpleja, Zarrin Rahnuma, Monideepa Mitra, Somen Roychowdhury, Prosanta Mondal
Publikováno v:
Journal of Primary Care Dentistry and Oral Health, Vol 5, Iss 3, Pp 113-116 (2024)
Orofacial clefts are one of the most common congenital defects that have a worldwide prevalence of 1 in 700 live births. Paul Tessier a French surgeon in 1976 classified this wide range of abnormalities into a simplified classification known as Tessi
Externí odkaz:
https://doaj.org/article/f6d4d3a5ffe84b568018a6d5cf50a480
Autor:
Azeez Alade, Peter Mossey, Waheed Awotoye, Tamara Busch, Abimbola M. Oladayo, Emmanuel Aladenika, Mojisola Olujitan, Emma Wentworth, Deepti Anand, Thirona Naicker, Lord J. J. Gowans, Mekonen A. Eshete, Wasiu L. Adeyemo, Erliang Zeng, Eric Van Otterloo, Michael O’Rorke, Adebowale Adeyemo, Jeffrey C. Murray, Justin Cotney, Salil A. Lachke, Paul Romitti, Azeez Butali
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Non-syndromic orofacial clefts (NSOFCs) are common birth defects with a complex etiology. While over 60 common risk loci have been identified, they explain only a small proportion of the heritability for NSOFCs. Rare variants have been impli
Externí odkaz:
https://doaj.org/article/95d6a791a7eb4ad7b423f503b9f69c2c
Akademický článek
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Autor:
Abimbola M. Oladayo, Oluwakemi Odukoya, Veronica Sule, Ikenna Molobe, Tamara Busch, Babatunde Akodu, Wasiu L. Adeyemo, Lord J. J. Gowans, Mekonen Eshete, Azeez Alade, Waheed Awotoye, Adebowale A. Adeyemo, Peter A. Mossey, Anya E. R. Prince, Jeffrey C. Murray, Azeez Butali
Publikováno v:
BMC Public Health, Vol 24, Iss 1, Pp 1-13 (2024)
Abstract Background A fundamental ethical issue in African genomics research is how socio-cultural factors impact perspectives, acceptance, and utility of genomic information, especially in stigmatizing conditions like orofacial clefts (OFCs). Previo
Externí odkaz:
https://doaj.org/article/4751704d52b040749b41c121b63e8a35
Autor:
Toshiyuki Itai, Fangfang Yan, Andi Liu, Yulin Dai, Chihiro Iwaya, Sarah W. Curtis, Elizabeth J. Leslie, Lukas M. Simon, Peilin Jia, Xiangning Chen, Junichi Iwata, Zhongming Zhao
Publikováno v:
HGG Advances, Vol 5, Iss 3, Pp 100313- (2024)
Summary: Orofacial clefts (OFCs) are common congenital birth defects with various etiologies, including genetic variants. Online Mendelian Inheritance in Man (OMIM) annotated several hundred genes involving OFCs. Furthermore, several hundreds of de n
Externí odkaz:
https://doaj.org/article/d1da2bc8f18746018552c2282332f15a
Autor:
Yulin Dai, Toshiyuki Itai, Guangsheng Pei, Fangfang Yan, Yan Chu, Xiaoqian Jiang, Seth M. Weinberg, Nandita Mukhopadhyay, Mary L. Marazita, Lukas M. Simon, Peilin Jia, Zhongming Zhao
Publikováno v:
HGG Advances, Vol 5, Iss 3, Pp 100312- (2024)
Summary: Orofacial clefts (OFCs) are among the most common human congenital birth defects. Previous multiethnic studies have identified dozens of associated loci for both cleft lip with or without cleft palate (CL/P) and cleft palate alone (CP). Alth
Externí odkaz:
https://doaj.org/article/1674e572859a430fb03d3eef41dde83f
Autor:
Marek Hampl, Nela Jandová, Denisa Lusková, Monika Nováková, Tereza Szotkowská, Štěpán Čada, Jan Procházka, Jiri Kohoutek, Marcela Buchtová
Publikováno v:
Disease Models & Mechanisms, Vol 17, Iss 6 (2024)
Externí odkaz:
https://doaj.org/article/da1c92341f2c4e39bd23cffe0800a750
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Several mutations in the IRF6 gene have been identified as a causative link to VWS. In this investigation, whole-exome sequencing (WES) and Sanger sequencing of a three-generation pedigree with an autosomal-dominant inheritance pattern affected by VW
Externí odkaz:
https://doaj.org/article/85824696cf694671bbcea7a36ea8aeca