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1.
Int J Pediatr Otorhinolaryngol ; 77(7): 1077-82, 2013 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-23684175

RESUMEN

OBJECTIVE: There are many hearing impaired individuals in Monte Santo, a rural municipality in the state of Bahia, Brazil, including multiple familial cases strongly suggestive of a genetic aetiology. METHODS: The present study investigated 81 subjects with hearing impairment (HI) recruited from 36 families. Mutations often associated with HI, i.e. the DFNB1 mutations c.35delG in GJB2, deletions del(GJB6-D13S1830) and del(GJB6-D13S1854), and A1555G in the mitochondrial gene MTRNR1 were initially analyzed, with additional mutations in GJB2 identified by sequencing the coding region of the gene. RESULTS: Seven different mutations were present in GJB2 with mutations c.35delG and p.Arg75Gln, which are known to be pathogenic, identified in 37.0% of the subjects. Individuals homozygous for the c.35delG mutation were diagnosed in eight families, corresponding to 24.7% of unrelated individuals with nonsyndromic hearing impairment (NSHI), and an additional heterozygote for this mutation was present in a single family. Ten individuals (12.4%) in another family were heterozygous for the mutation p.Arg75Gln. CONCLUSIONS: Significant heterogeneity was observed in the alleles and patterns of NSHI inheritance among the subjects studied, probably due to the extensive inter-ethnic admixture that characterizes the peoples of Brazil, together with a high prevalence of community endogamy and consanguineous marriage.


Asunto(s)
Conexinas/genética , Etnicidad/genética , Pérdida Auditiva/etnología , Pérdida Auditiva/genética , Mutación , Población Rural/estadística & datos numéricos , Adolescente , Adulto , Anciano , Brasil/epidemiología , Niño , Preescolar , Conexina 26 , Conexina 30 , Consanguinidad , Femenino , Humanos , Masculino , Persona de Mediana Edad , Receptores Nucleares Huérfanos/genética , Reacción en Cadena de la Polimerasa , Polimorfismo de Longitud del Fragmento de Restricción , Adulto Joven
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