Abstract
AbstractThe study was carried out in children born during the four year period 1981–1984 in the Greater Manchester County. The children were investigated for possible congenital infections. Perinatal assessment was carried out for adverse aetiological factors. Family histories were obtained and parents and siblings were examined for any hearing impairment. A total of 164 cases were investigated. Various aetiological groups were formed which showed the following distribution: cause unknown 36.5 per cent; genetic group 20.1 per cent; adverse perinatal factors 14.6 per cent; congenital infections 9.8 per cent; meningitis 6.1 per cent; chromosomal abnormalities 3.7 per cent; syndromal group 3.7 per cent; and miscellaneous 5.5 per cent. The findings are discussed in the light of previous studies.
Publisher
Cambridge University Press (CUP)
Subject
Otorhinolaryngology,General Medicine
Reference21 articles.
1. A simple method of estimating the segregation ratio under complete ascertainment;Li;American Journal of Human Genetics,1968
2. Genetic heterogeneity in Waardenburg Syndrome;Arias;Birth Defects: Original Article Series,1971
3. Aetiology of bilateral sensori-neural hearing loss in young children;Newton;Journal of Laryngology and Otology,1985
4. A study of the causes of hearing loss in a population of deaf children with special reference to genetic factors
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