K otázce etiologie vrozeného postizení sluchu u dĕtí
[Etiology of congenital hearing disorders in children]
Jazyk čeština Země Česko Médium print
Typ dokumentu anglický abstrakt, časopisecké články
PubMed
2225166
- MeSH
- dítě MeSH
- hluchota vrozené etiologie genetika MeSH
- lidé MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- Publikační typ
- anglický abstrakt MeSH
- časopisecké články MeSH
The author analyzes factors which may play a part in the aetiology of severe congenital bilateral perception deafness--practically complete deafness--in children. The group of patients comprises 177 deaf children, 135 siblings with normal hearing and 70 deaf parents and other relatives. Pathological factors during pregnancy were detected in 20, perinatal and neonatal pathology in 32 instances. If the anamnestically detected risk factors in the aetiology of the hearing deficit played a part, theoretically by their elimination a considerable proportion of the congenital hearing affections in children could be prevented. The author emphasizes the necessity of collaboration with a geneticist in the prevention of inborn hereditary deafness.