Literature DB >> 19930248

Fitness among individuals with early childhood deafness: Studies in alumni families from Gallaudet University.

Susan H Blanton1, Walter E Nance, Virginia W Norris, Katherine O Welch, Amber Burt, Arti Pandya, Kathleen S Arnos.   

Abstract

The genetic fitness of an individual is influenced by their phenotype, genotype and family and social structure of the population in which they live. It is likely that the fitness of deaf individuals was quite low in the Western European population during the Middle Ages. The establishment of residential schools for deaf individuals nearly 400 years ago resulted in relaxed genetic selection against deaf individuals which contributed to the improved fitness of deaf individuals in recent times. As part of a study of deaf probands from Gallaudet University, we collected pedigree data, including the mating type and the number and hearing status of the children of 686 deaf adults and 602 of their hearing siblings. Most of these individuals had an onset of severe to profound hearing loss by early childhood. Marital rates of deaf adults were similar to their hearing siblings (0.83 vs. 0.85). Among married individuals, the fertility of deaf individuals is lower than their hearing siblings (2.06 vs. 2.26, p = 0.005). The fitness of deaf individuals was reduced (p = 0.002). Analysis of fertility rates after stratification by mating type reveals that matings between two deaf individuals produced more children (2.11) than matings of a deaf and hearing individual (1.85), suggesting that fertility among deaf individuals is influenced by multiple factors.

Entities:  

Mesh:

Year:  2009        PMID: 19930248      PMCID: PMC2804774          DOI: 10.1111/j.1469-1809.2009.00553.x

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


  24 in total

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Authors:  Q J Wang; C Y Lu; N Li; S Q Rao; Y B Shi; D Y Han; X Li; J Y Cao; L M Yu; Q Z Li; M X Guan; W Y Yang; Y Shen
Journal:  J Med Genet       Date:  2004-06       Impact factor: 6.318

4.  Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians.

Authors:  M Tekin; N Akar; S Cin; S H Blanton; X J Xia; X Z Liu; W E Nance; A Pandya
Journal:  Hum Genet       Date:  2001-05       Impact factor: 4.132

5.  Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population.

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Journal:  Am J Med Genet       Date:  2000-01-17

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7.  Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.

Authors:  Arti Pandya; Kathleen S Arnos; Xia J Xia; Katherine O Welch; Susan H Blanton; Thomas B Friedman; Guillermina Garcia Sanchez; Xiu Z Liu MD; Robert Morell; Walter E Nance
Journal:  Genet Med       Date:  2003 Jul-Aug       Impact factor: 8.822

8.  Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India.

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9.  A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart.

Authors:  Kathleen S Arnos; Katherine O Welch; Mustafa Tekin; Virginia W Norris; Susan H Blanton; Arti Pandya; Walter E Nance
Journal:  Am J Hum Genet       Date:  2008-07-24       Impact factor: 11.025

10.  Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study.

Authors:  Ignacio Del Castillo; Miguel A Moreno-Pelayo; Francisco J Del Castillo; Zippora Brownstein; Sandrine Marlin; Quint Adina; David J Cockburn; Arti Pandya; Kirby R Siemering; G Parker Chamberlin; Ester Ballana; Wim Wuyts; Andréa Trevas Maciel-Guerra; Araceli Alvarez; Manuela Villamar; Mordechai Shohat; Dvorah Abeliovich; Hans-Henrik M Dahl; Xavier Estivill; Paolo Gasparini; Tim Hutchin; Walter E Nance; Edi L Sartorato; Richard J H Smith; Guy Van Camp; Karen B Avraham; Christine Petit; Felipe Moreno
Journal:  Am J Hum Genet       Date:  2003-10-21       Impact factor: 11.025

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  4 in total

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Journal:  PLoS One       Date:  2014-11-06       Impact factor: 3.240

2.  Childhood hearing impairment and fertility in Norway.

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Journal:  Sci Rep       Date:  2022-01-10       Impact factor: 4.379

3.  Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population.

Authors:  Georgii P Romanov; Anna A Smirnova; Vladimir I Zamyatin; Aleksey M Mukhin; Fedor V Kazantsev; Vera G Pshennikova; Fedor M Teryutin; Aisen V Solovyev; Sardana A Fedorova; Olga L Posukh; Sergey A Lashin; Nikolay A Barashkov
Journal:  Biology (Basel)       Date:  2022-02-07

4.  Deaf intermarriage has limited effect on the prevalence of recessive deafness and no effect on underlying allelic frequency.

Authors:  Derek C Braun; Samir Jain; Eric Epstein; Brian H Greenwald; Brienna Herold; Margaret Gray
Journal:  PLoS One       Date:  2020-11-04       Impact factor: 3.240

  4 in total

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