Literature DB >> 17152466

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

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

Abstract

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 hearing carrying abnormal gene can help avoid birth of deaf children.

Entities:  

Mesh：

Substances：

Year:  2006        PMID： 17152466

Source DB:  PubMed          Journal:  Vestn Otorinolaringol        ISSN： 0042-4668


  1 in total

1.  Update of the GJB2/DFNB1 mutation spectrum in Russia: a founder Ingush mutation del(GJB2-D13S175) is the most frequent among other large deletions.

Authors:  Elena A Bliznetz; Maria R Lalayants; Tatiana G Markova; Oleg P Balanovsky; Elena V Balanovska; Roza A Skhalyakho; Elvira A Pocheshkhova; Natalya V Nikitina; Sergey V Voronin; Elena K Kudryashova; Oleg S Glotov; Alexander V Polyakov
Journal:  J Hum Genet       Date:  2017-04-13       Impact factor: 3.172
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.