Literature DB >> 15185405

Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness.

Saida Ben Arab1, Saber Masmoudi, Najeh Beltaief, Slah Hachicha, Hammadi Ayadi.   

Abstract

Deafness is an important health problem in the Tunisian population, especially in isolates where the prevalence ranges from 2 to 8%. To evaluate the effect of inbred unions on deafness, a study was conducted on 5,020 individuals (160 are deaf) between 2000 and 2002 in the North of Tunisia. The coefficient of inbreeding for all individuals and the levels of inbreeding in ten districts were computed. The higher levels were obtained in the rural districts. Our study revealed that geographic isolation, social traditions, and parental involvement in mode selection all contribute to increase consanguinity in these regions. The mean inbreeding seems to be similar to those estimated in highly inbred isolates in the world. The relative risk of the 35delG mutation, the single most frequent allele for non-syndromic recessive deafness in Tunisia, was estimated from the observed inbreeding coefficient and found to be 10.76 (SD 7.74) for first-cousin marriages, which are the most common form of consanguineous marriage encountered. Our knowledge of the risk rate of deafness and our understanding of consanguinity is required for the prevention of genetic deafness in the Tunisian population. Copyright 2004 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2004        PMID: 15185405     DOI: 10.1002/gepi.10321

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  16 in total

1.  Consanguinity, endogamy, and genetic disorders in Tunisia.

Authors:  Nizar Ben Halim; Nissaf Ben Alaya Bouafif; Lilia Romdhane; Rym Kefi Ben Atig; Ibtissem Chouchane; Yosra Bouyacoub; Imen Arfa; Wafa Cherif; Sonia Nouira; Faten Talmoudi; Khaled Lasram; Sana Hsouna; Welid Ghazouani; Hela Azaiez; Leila El Matri; Abdelmajid Abid; Neji Tebib; Marie-Françoise Ben Dridi; Salem Kachboura; Ahlem Amouri; Mourad Mokni; Saida Ben Arab; Koussay Dellagi; Sonia Abdelhak
Journal:  J Community Genet       Date:  2012-12-04

2.  Inter-ethnic differences in genetic polymorphisms of xenobiotic-metabolizing enzymes (CYP1A1, CYP2D6, NAT1 and NAT2) in healthy populations: correlation with the functional in silico prediction.

Authors:  Rim Khlifi; Ghada Ben Salah; Amine Chakroun; Amel Hamza-Chaffai; Ahmed Rebai
Journal:  Mol Biol Rep       Date:  2014-06-17       Impact factor: 2.316

3.  High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects.

Authors:  Mariem Ben Saïd; Mounira Hmani-Aifa; Imen Amar; Shahid Mahmood Baig; Mirna Mustapha; Sedigheh Delmaghani; Abdelaziz Tlili; Abdelmonem Ghorbel; Hammadi Ayadi; Guy Van Camp; Richard J H Smith; Mustafa Tekin; Saber Masmoudi
Journal:  Genet Test Mol Biomarkers       Date:  2010-06

4.  Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria.

Authors:  Nadege Kammoun Jellouli; Ikhlass Hadj Salem; Emna Ellouz; Zeineb Kamoun; Fatma kamoun; Abdelaziz tlili; Naziha Kaabachi; Chanez Triki; Faiza Fakhfakh
Journal:  J Hum Genet       Date:  2014-02-27       Impact factor: 3.172

5.  Interplay of socio-economic factors, consanguinity, fertility, and offspring mortality in Monastir, Tunisia.

Authors:  Emna Kerkeni; Kamel Monastiri; Besma Saket; Mohamed Neji Guediche; Hassen Ben Cheikh
Journal:  Croat Med J       Date:  2007-10       Impact factor: 1.351

6.  A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60.

Authors:  Mariem Ben Said; M'hamed Grati; Takahiro Ishimoto; Bing Zou; Imen Chakchouk; Qi Ma; Qi Yao; Bouthaina Hammami; Denise Yan; Rahul Mittal; Noritaka Nakamichi; Abdelmonem Ghorbel; Lingling Neng; Mustafa Tekin; Xiao Rui Shi; Yukio Kato; Saber Masmoudi; Zhongmin Lu; Mounira Hmani; Xuezhong Liu
Journal:  Hum Genet       Date:  2016-03-29       Impact factor: 4.132

7.  Prevalence of prelingual deafness in Italy.

Authors:  L Bubbico; A Rosano; A Spagnolo
Journal:  Acta Otorhinolaryngol Ital       Date:  2007-02       Impact factor: 2.124

8.  Consanguinity and reproductive health among Arabs.

Authors:  Ghazi O Tadmouri; Pratibha Nair; Tasneem Obeid; Mahmoud T Al Ali; Najib Al Khaja; Hanan A Hamamy
Journal:  Reprod Health       Date:  2009-10-08       Impact factor: 3.223

Review 9.  Genetics and meta-analysis of recessive non-syndromic hearing impairment and Usher syndrome in Maghreb population: lessons from the past, contemporary actualities and future challenges.

Authors:  Amal Souissi; Abdullah A Gibriel; Saber Masmoudi
Journal:  Hum Genet       Date:  2021-07-15       Impact factor: 4.132

10.  Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population.

Authors:  Amal Souissi; Mariem Ben Said; Ikhlas Ben Ayed; Ines Elloumi; Amal Bouzid; Mohamed Ali Mosrati; Mehdi Hasnaoui; Malek Belcadhi; Nabil Idriss; Hassen Kamoun; Nourhene Gharbi; Abdullah A Gibriel; Abdelaziz Tlili; Saber Masmoudi
Journal:  J Adv Res       Date:  2021-01-12       Impact factor: 10.479

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.