Analysis of Consanguinity as Risk Factor of Nonsyndromic Cleft Lips with or without Palate
Hutami I.R., Fatimah-Muis S., Rochmah Y.S., Harumsari S., Christiono S., Faradz S.M.H.
Abstract
Objectives The etiologies of nonsyndromic cleft lips with or without palate (NS CL/P) are multifactorial, which include consanguineous marriages. The incidence of NS CL/P is relatively high in Indonesia notably in one of Indonesia's tribes whose members frequently marry close cousins. Thus, the purpose of this study is to analysis consanguinity as risk factor of NS CL/P in Sasak tribe, East Lombok, Indonesia Materials and Methods An observational analysis was made of a collected database of NS CL/P patients treated in social services in regency hospital of Dr. Soejono Selong, East Lombok, Indonesia. Demographic data such as age, gender, address (urban/rural), parent's education, presence or absence of consanguinity, type of clefts, and a three-generation pedigree were collected by interview and hospital medical record. Before analysis, patient information was anonymized and deidentified. From 2016 to 2018, each of 100 cleft and normal subjects with their Sasak parent were audited. The risk factors were analyzed statistically using odds ratio (OR) and chi-squared test. Results Consanguineous marriages identified 54 cases (54%), and 10 cases (10%) out of a total each 100 NS CL/P and controls, respectively. The majority of consanguinity (53.7%) was discovered in marriages between first cousins. NS CL/P cases were statistically linked (p = 0.00) with consanguineous marriages (OR: 10; 95% confidence interval: 1.6-3.1); in which the most prevalent case is unilateral cleft lips. Conclusion Consanguineous marriage increases the risk of NS CL/P in Sasak tribe, East Lombok, Indonesia. The development of strategies to educate communities on the impacts of culture-consanguineous marriage is required. The genetic inheritance from their ancestor may be responsible for the increased incidence of NS CL/P.
Orofacial Cleft Frequency Differences Depending on Geographic Origin: Coast vs. Inland
Filgueiras V.M., Filho V.V.L., Furtado P.G.C., Lacerda R.H.W., Luna A.M., Pereira J.A.T., Tenorio I.S., Vieira A.R., Vieira A.R.
Orofacial Cleft and Mandibular Prognathism—Human Genetics and Animal Models
Jaruga A., Ksiazkiewicz J., Ksiazkiewicz J., Kuzniarz K., Tylzanowski P., Tylzanowski P.
Maternal polymorphism MTHFR A1298C not C677T and MSX1 as the risk factors of non-syndrome cleft lips /palate in sasak tribe Indonesia
Faradz S.M.H., Fatimah-Muis S., Harumsari S., Rochmah Y.S., Sosiawan A., Suwarsi L.
The role of CNVs in the etiology of rare autosomal recessive disorders: The example of TRAPPC9-associated intellectual disability
Busa T., Cacciagli P., Coubes C., Duffourd Y., Duffourd Y., Gatinois V., Germain D.P., Germain D.P., Missirian C., Mortreux J., Nadeau G., Philip N., Philip N., Pinard J.-M., Puechberty J., Sanlaville D., Sanlaville D., Sanlaville D., Tevissen H., Villard L.
Consanguineous Marriages and Dental Anomalies: A Cross-Sectional Analytical Study
Abbas B., Abbas S., Khurshid Z., Malik S.M., Rahim M., Umair M.
Genetic and reproductive consequences of consanguineous marriage in Bangladesh
Anwar S., Arafat Y., Hosen M.J., Mourosi J.T.
A likelihood ratio approach for identifying three-quarter siblings in genetic databases
Barcelo-Vidal C., de Cid R., Galvan-Femenia I., Galvan-Femenia I., Graffelman J., Graffelman J., Moreno V., Moreno V., Moreno V., Moreno V., Sumoy L.
Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis
Gersak K., Gersak K., Karas Kuzelicki N., Locatelli I., Slavec L., Slavec L.
The genetic aspect of non-syndromic cleft lip and palate towards candidate genes in the etiology: a literature review
Kurniati M., Pramono D.R., Sosiawan A., Tirtaningsih N.W.
Genetic factors in nonsyndromic orofacial clefts
Cs P., Khan M.I., Srinath N.M.