Literature DB >> 7856647

Epidemiological and genetic studies of congenital profound deafness in the general population of Sichuan, China.

X Liu1, L Xu, S Zhang, Y Xu.   

Abstract

People with congenital profound deafness (CPD) were surveyed in the general population of Sichuan. The prevalence was 0.082% (104/126, 876) of the general population, male 0.086%, female 0.078%. There was no significant difference in prevalence between urban and rural populations. However the population living in the mountains had a much higher prevalence than people from the foothills and plains (P < 0.05). Amongst the nationalities investigated, there were significant differences in prevalence. Non-Chinese, except for Tibetans, presented a significantly higher prevalence than Han Chinese. There was a significantly higher prevalence among the inbred population (0.82%) than among the non-inbred population (0.72%). An effect of parental age was demonstrated, but no effect of birth order was found. There was a significant seasonal variation in prevalence. Inherited cases could account for 71.2% of all cases, of which 92% were autosomal recessive (AR) and 8% autosomal dominant (AD). Heterogeneity in AR was found with at least 8 different loci. The fitness was 60.26%, the coefficient of selection was 0.3974, mutation rate was estimated to be 2.0 x 10(-4), and no heterozygote advantage was proven.

Entities:  

Mesh:

Year:  1994        PMID: 7856647     DOI: 10.1002/ajmg.1320530214

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

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

Authors:  Susan H Blanton; Walter E Nance; Virginia W Norris; Katherine O Welch; Amber Burt; Arti Pandya; Kathleen S Arnos
Journal:  Ann Hum Genet       Date:  2009-11-20       Impact factor: 1.670

Review 2.  Genetics of hearing and deafness.

Authors:  Simon Angeli; Xi Lin; Xue Zhong Liu
Journal:  Anat Rec (Hoboken)       Date:  2012-10-08       Impact factor: 2.064

3.  Novel GRHL2 Gene Variant Associated with Hearing Loss: A Case Report and Review of the Literature.

Authors:  Katarina Trebusak Podkrajsek; Tine Tesovnik; Nina Bozanic Urbancic; Saba Battelino
Journal:  Genes (Basel)       Date:  2021-03-26       Impact factor: 4.096

4.  Diagnosis and Treatment of Congenital Sensorineural Hearing Loss.

Authors:  Divya A Chari; Dylan K Chan
Journal:  Curr Otorhinolaryngol Rep       Date:  2017-09-30

5.  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

Review 6.  The Importance of Early Genetic Diagnostics of Hearing Loss in Children.

Authors:  Nina Božanić Urbančič; Saba Battelino; Tine Tesovnik; Katarina Trebušak Podkrajšek
Journal:  Medicina (Kaunas)       Date:  2020-09-14       Impact factor: 2.430

  6 in total

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