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Article

[Genetic screening among children with congenital and early childhood hearing loss].

Vestnik otorinolaringologii - 1 Jan 2006

Markova T G, Nekrasovan V M V, Shagina I A, Poliakov A A

Abstract excerpt

Prevalence of mutations of genes of connexin 26, connexin 30 and mitochondrial DNA was studied among children with congenital and early childhood hearing loss. Screening with available methods of DNA diagnosis was conducted in some specialized schools. It was found that genetic disorders among children with congenital and early childhood hearing loss are rather frequent. Genetic consulting of parents with normal...

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Identifiers

PMID: 17152466

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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