Fundamento y objetivo: La mutación AG del genoma mitocondrial causa hipoacusia neurosensorial y ototoxicidad familiar por aminoglucósidos. Pacientes. Qué es la sordera súbita y por qué hay que tener cuidado con los medicamentos ototóxicos, que dañan las células sensoriales del oído. Debe descartarse la presenciade la mutación AG en pacientes conantecedentes de hipoacusia por vía maternaantes de administrar aminoglucósidos.

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Ototoxucos Pages Screening for the AG mutation was performed on 72 patients with nonsyndromic sensorineural hearing loss. O uso desses medicamentos por pelo menos 15 dias foi identificado em 43 casos. The AG mutation in the mitochondrial genome causes sensorineural hearing loss and familial aminoglycoside ototoxicity.

These manuscripts contain updated topics with a major clinical or conceptual relevance in modern medicine. Cigarette smoking and risk for hearing impairment: Hearing loss and nephrotoxicity in long-term aminoglycoside treatment in patients with tuberculosis.

Cigarette smoking and hearing loss: Em um estudo de coorte entre eforam registrados 2. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

Sintomas auditivos ou vestibulares, como o zumbido, a tontura ou mesmo o relato de pequena dificuldade em ouvir, devem ser valorizados pelos profissionais envolvidos.

Comparative uptake of gentamicin, netilmicin, and amikacin in the guinea pig cochlea and vestibule. Services on Demand Journal.


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hipoacusia por ototoxicos pdf

Isr Med Assoc J. Are you a health professional able to prescribe or dispense drugs? Agradecemos aos profissionais e pacientes dos hospitais participantes. How to cite this article. This item has received. Show more Show less. Familial susceptibility to aminoglycoside ototoxicity due to the AG mutation in the mitochondrial DNA. The AG mutation should be screened in individuals with maternal relatives with hearing loss before administering aminoglycosides.

World health organization [homepage on the Internet].

The AG mutation was identified in 15 patients Os achados do presente estudo foram semelhantes aos de Carmo et al. Individuals with the AG mutation that had been treated with aminoglycosides developed more severe hearing loss. SCS Quadra 1, Bl. Continuing navigation will hhipoacusia considered as acceptance of this use.

SRJ is a prestige metric based hipkacusia the idea that not all citations are the same. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. International Union against Tuberculosis and Lung Disease. Subscriber If you already have your login data, please click here. Epidemiological profile of hospitalized patients with TB at a referral hospital in the city of Rio de Janeiro, Brazil.

The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years. R Ci Med Biol.


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J Occup Environ Med. Agradecimentos Agradecemos hipocusia profissionais e pacientes dos hospitais participantes. Os pacientes foram divididos em dois grupos: Audiometria; Perda auditiva; Tuberculose; Toxicidade de drogas. Duggal P, Sarkar M. World health organization [cited Aug 15]. Audiologic monitoring of multi-drug resistant tuberculosis patients on aminoglycoside treatment with long term follow-up.

Os participantes foram entrevistados e realizaram audiometria tonal liminar. Epidemiologic basis of tuberculosis control. Rev Bras Penumol Sanit.

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Se continuar a navegar, consideramos que aceita o seu uso. Int J Tuberc Lung Dis. You can change the settings or obtain more information by clicking here. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. Previous article Next article. A five-year longitudinal study of hearing in a Danish rural population aged years. The journal adheres to the standards of academic research publications in all aspects including peer-review and ethical principles.

All of them presented maternal relatives with deafness.