Literature DB >> 17331080

The fate of 12 recessive mutations in a single village.

J Zlotogora1, Y Hujerat, S Barges, S A Shalev, A Chakravarti.   

Abstract

In a Muslim Arab village, relatively isolated because of the preference of consanguineous marriages, we studied the fate of 12 mutations in 5 different genes. The study was based on carriers detected among relatives of affected patients and of carriers discovered in a random sample of 424 adults. Most of the mutations have been introduced by a carrier(s) originating from another village, but a few have been de novo events. Mutations that are very frequent in the entire village were introduced soon after the foundation of the village. Examples of such mutations are [GBJ2, 35Gdel] and [MEFV, M680I], with a carrier frequency of 7.8% and 6.2%, respectively. Many of the other mutations that are rare were introduced recently into the village and are frequent only among the descendants of the first couple carrying the mutation. For instance all the carriers of [ARSA, Q190H], responsible for metachromatic leukodystrophy, were found among the 218 descendants of a couple who were living in the village 4 generations ago. Since the village is typical for the region this study allows for some general conclusions to be drawn. In a population with a high degree of inbreeding the diagnosis of a single family with a patient(s) affected with a recessive disorder points to a recent event, while the finding of a rare disease in several families from an inbred population points to an older mutation. Mutations are often "exported" from one population to another by marriage. In the new inbred population this novel mutation will either be lost or will become frequent as the result of a founder effect. These observations are important for genetic counselling in the case of a recent mutation, since only the descendants of the founder couple are at risk, while in the case of older mutations the risk may be for the entire village. In the case of those frequent ancient mutations, the risk for a relative of an affected individual will be similar whether he marries a close relative or any random individual in the village.

Entities:  

Mesh:

Year:  2007        PMID: 17331080     DOI: 10.1111/j.1469-1809.2006.00308.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  9 in total

1.  Compound heterozygosity for three common MEFV mutations in a highly consanguineous family with familial Mediterranean fever.

Authors:  H Seidel; O K Steinlein
Journal:  Eur J Pediatr       Date:  2007-08-04       Impact factor: 3.183

2.  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

3.  Report of a Second Lebanese Family with Basel-Vanagaite-Smirin-Yosef Syndrome: Possible Founder Mutation.

Authors:  Pratibha Nair; Sandra Sabbagh; Sami Bizzari; Florian Brunner; Samantha Stora; Mahmoud T Al-Ali; Martin Gencik; Stephany El-Hayek; André Mégarbané
Journal:  Mol Syndromol       Date:  2019-06-28

Review 4.  The molecular basis of autosomal recessive diseases among the Arabs and Druze in Israel.

Authors:  Joël Zlotogora
Journal:  Hum Genet       Date:  2010-09-18       Impact factor: 4.132

5.  Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran.

Authors:  Christina M Sloan-Heggen; Mojgan Babanejad; Maryam Beheshtian; Allen C Simpson; Kevin T Booth; Fariba Ardalani; Kathy L Frees; Marzieh Mohseni; Reza Mozafari; Zohreh Mehrjoo; Leila Jamali; Saeideh Vaziri; Tara Akhtarkhavari; Niloofar Bazazzadegan; Nooshin Nikzat; Sanaz Arzhangi; Farahnaz Sabbagh; Hasan Otukesh; Seyed Morteza Seifati; Hossein Khodaei; Maryam Taghdiri; Nicole C Meyer; Ahmad Daneshi; Mohammad Farhadi; Kimia Kahrizi; Richard J H Smith; Hela Azaiez; Hossein Najmabadi
Journal:  J Med Genet       Date:  2015-10-07       Impact factor: 6.318

Review 6.  Evolution in health and medicine Sackler colloquium: Consanguinity, human evolution, and complex diseases.

Authors:  A H Bittles; M L Black
Journal:  Proc Natl Acad Sci U S A       Date:  2009-09-23       Impact factor: 11.205

7.  The Israeli National Genetic database: a 10-year experience.

Authors:  Joël Zlotogora; George P Patrinos
Journal:  Hum Genomics       Date:  2017-03-16       Impact factor: 4.639

8.  Consanguinity and rare neurological disease. A five year experience from the Korle Bu Teaching Hospital, Accra, Ghana.

Authors:  E V Badoe
Journal:  eNeurologicalSci       Date:  2016-01-22

9.  Controversies and considerations regarding the termination of pregnancy for foetal anomalies in Islam.

Authors:  Abdulrahman Al-Matary; Jaffar Ali
Journal:  BMC Med Ethics       Date:  2014-02-05       Impact factor: 2.652

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.