Literature DB >> 30891741

Consanguinity: A blessing or menace at population level?

Munir Ahmad Bhinder1, Haleema Sadia2, Nasir Mahmood3, Muhammad Qasim4, Zawar Hussain5, Muhammad Mudassar Rashid1, Muhammad Yasir Zahoor6, Rashid Bhatti7, Wasim Shehzad6, Ali Muhammad Waryah8, Shah Jahan3.   

Abstract

Consanguinity has highly complex and multifaceted aspects with sociocultural as well as biological debates on its pros and cons. The biological upshot of consanguinity includes the increased homozygosity, which results in manifold increased risk of genetic disorders at family and population levels. On the other hand, in addition to social, cultural, political, and economic benefits, consanguineous marriages have biological advantages at the population level. The consequence of consanguineous marriages is an upsurge in the number of homozygous diseased individuals with fewer chances of mating and reduced chances of survival, therefore evolutionarily confining the transmission of disease alleles to future generations and encouraging its elimination from a population. Protective effects of consanguinity have also been observed in a few diseases in different populations. Although attractive for many reasons, nonconsanguineous marriages will cause risk alleles to spread throughout the population, making most individuals carriers, and ultimately will resume the production of recessive diseases in subsequent generations. Although consanguinity, from an evolutionary point of view, is beneficial at the population level, it increases the risk of diseases in the very next generation. Presently, there is no treatment for most of the genetic disorders; we cannot opt for consanguinity for long-term benefits. Nonconsanguineous marriages are a better strategy by which we may delay disease manifestation for some generations until science offers a viable solution.
© 2019 John Wiley & Sons Ltd/University College London.

Entities:  

Keywords:  consanguinity; disease allele; evolution; genetic counseling; homozygosity; recessive genetic disorders

Mesh:

Year:  2019        PMID: 30891741     DOI: 10.1111/ahg.12308

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


  5 in total

1.  Investigating the genetic profile of familial atypical cystic fibrosis patients (DeltaF508-CFTR) with neonatal biliary atresia.

Authors:  Omar Rabab'h; Dunia Aburizeg; Eyad Altamimi; Lynn Akasheh; Zain Dardas; Luma Srour; Heyam Awad; Bilal Azab
Journal:  J Appl Genet       Date:  2022-10-07       Impact factor: 2.653

2.  Consanguineous Marriages and Dental Anomalies: A Cross-Sectional Analytical Study.

Authors:  Beenish Abbas; Sana Abbas; Saadia Muneer Malik; Majida Rahim; Muhammad Umair; Zohaib Khurshid
Journal:  Int J Dent       Date:  2022-04-06

3.  Screening of BRCA1/2 variants in Mauritanian breast cancer patients.

Authors:  Selma Mohamed Brahim; Ekht Elbenina Zein; Crystel Bonnet; Cheikh Tijani Hamed; Malak Salame; Mohamed Vall Zein; Meriem Khyatti; Ahmedou Tolba; Ahmed Houmeida
Journal:  BMC Cancer       Date:  2022-07-20       Impact factor: 4.638

Review 4.  Genetic etiology of hereditary hearing loss in the Gulf Cooperation Council countries.

Authors:  Abdullah Al Mutery; Mona Mahfood; Jihen Chouchen; Abdelaziz Tlili
Journal:  Hum Genet       Date:  2021-08-02       Impact factor: 4.132

5.  Mutational spectrum of SMPD1 gene in Pakistani Niemann-Pick disease patients.

Authors:  Huma Arshad Cheema; Iqra Ghulam Rasool; Muhammad Nadeem Anjum; Muhammad Yasir Zahoor
Journal:  Pak J Med Sci       Date:  2020 Mar-Apr       Impact factor: 1.088

  5 in total

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