Literature DB >> 6619650

Childhood deafness in southern Africa. An aetiological survey of 3,064 deaf children.

S Sellars, P Beighton.   

Abstract

We have completed a survey of the causes of deafness in 3,064 children with defective hearing who attend special schools in Southern Africa. Specific genetic or multifactorial syndromes were diagnosed in 7 per cent, familial undifferentiated deafness was recognized in 11 per cent, while in 25 per cent the deafness was acquired.

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Year:  1983        PMID: 6619650     DOI: 10.1017/s0022215100095736

Source DB:  PubMed          Journal:  J Laryngol Otol        ISSN: 0022-2151            Impact factor:   1.469


  3 in total

1.  Familial streptomycin ototoxicity in a South African family: a mitochondrial disorder.

Authors:  J C Gardner; R Goliath; D Viljoen; S Sellars; G Cortopassi; T Hutchin; J Greenberg; P Beighton
Journal:  J Med Genet       Date:  1997-11       Impact factor: 6.318

2.  Community-based infant hearing screening for early detection of permanent hearing loss in Lagos, Nigeria: a cross-sectional study.

Authors:  B O Olusanya; S L Wirz; L M Luxon
Journal:  Bull World Health Organ       Date:  2008-12       Impact factor: 9.408

3.  Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.

Authors:  L A Farrer; K M Grundfast; J Amos; K S Arnos; J H Asher; P Beighton; S R Diehl; J Fex; C Foy; T B Friedman
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

  3 in total

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