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Braz J Otorhinolaryngol ; 77(5): 573-6, 2011.
Artigo em Inglês, Português | MEDLINE | ID: mdl-22030963

RESUMO

UNLABELLED: Streptomycin and aminoglycoside derivatives are commonly used to treat tuberculosis and other stubborn infections; these drugs may alter auditory and/or vestibular function. Mutations in mitochondrial DNA have been associated with hypersensitivity to aminoglycosides; no studies have been conducted in Mexicans, which are very prone to such alterations because aminoglycosides have been prescribed carelessly for many years, irrespective of the ailment to be treated. AIM: We investigated "hot spot" mutations described previously as causing inner ear alterations. METHODS: Hot spot mutations at the 12S rRNA gene and the tRNA Serine (UCN) gene were screened by PCR-RFLP and sequencing in 65 subjects undergoing audiological and vestibular testing. STUDY DESIGN: Experimental. RESULTS: 32 individuals had healthy auditory and vestibular function, whereas 33 subjects had auditory affections. We found none of the previously reported mutations related to aminoglycoside hypersensitivity, or non-syndromic hearing loss. Two hearing-impaired patients that had been treated with streptomycin had the T1189C variant of the mitochondrial 12S rRNA region. CONCLUSION: Mutations related to hearing loss in other ethnic backgrounds were not found in Mexicans. However, the T1189C variant is possibly a putative mutation related to aminoglycoside hypersensitivity and was present in 2 patients.


Assuntos
Aminoglicosídeos/efeitos adversos , DNA Mitocondrial/efeitos dos fármacos , Perda Auditiva/induzido quimicamente , Mutação Puntual/efeitos dos fármacos , RNA Ribossômico/efeitos dos fármacos , RNA de Transferência de Serina/efeitos dos fármacos , Adolescente , Adulto , Idoso , Criança , Pré-Escolar , Análise Mutacional de DNA , DNA Mitocondrial/genética , Predisposição Genética para Doença , Perda Auditiva/genética , Humanos , México , Pessoa de Meia-Idade , Mutação Puntual/genética , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , RNA Ribossômico/genética , RNA de Transferência de Serina/genética , Estreptomicina/efeitos adversos , Adulto Jovem
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