Screening of mutations of deafness-related genes in women of child-bearing age from Shijiazhuang area / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 462-465, 2016.
Article
em Zh
| WPRIM
| ID: wpr-247657
Biblioteca responsável:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To screen for mutations of deafness-related genes among ethic Chinese women of child-bearing age.</p><p><b>METHODS</b>In 324 women, 9 mutational sites in 4 deafness-related genes (SLC26A4, GJB3, GJB2 and mtDNA 12s rRNA) were screened using a gene chip.</p><p><b>RESULTS</b>Twenty women (6.17%) have carried mutations. These included 11 (3.40%) carrying a GJB2 gene mutation, 7 (2.16%) carrying a SLC26A4 gene mutation, 1 (0.31%) simultaneously carrying GJB3 and GJB2 gene mutations, and 1 (0.31%) carrying a mtDNA 12s rRNA gene mutation.</p><p><b>CONCLUSION</b>Women of child-bearing age have a high rate for carrying mutations of common deafness-related genes, among which 235delC in GJB2 was most common. Prenatal screening of couples with normal hearing is an effective way to prevent birth of affected children.</p>
Texto completo:
1
Base de dados:
WPRIM
Assunto principal:
Conexinas
/
Surdez
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Conexina 26
/
Genética
/
Mutação
Tipo de estudo:
Diagnostic_studies
/
Screening_studies
Aspecto:
Ethics
Limite:
Adult
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Female
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Humans
Idioma:
Zh
Revista:
Chinese Journal of Medical Genetics
Ano de publicação:
2016
Tipo de documento:
Article