Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Year range
1.
Int. arch. otorhinolaryngol. (Impr.) ; 19(2): 135-140, Apr-Jun/2015. tab, graf
Article in English | LILACS | ID: lil-747143

ABSTRACT

Introduction Mercury poisoning causes hearing loss in humans and animals. Acute and long-term exposures produce irreversible peripheral and central auditory system damage, and mercury in its various forms of presentation in the environment is ototoxic. Objective We investigated the otoacoustic emissions responses in a riverside population exposed to environmental mercury by analyzing the inhibitory effect of the medial olivocochlear system (MOCS) on transient otoacoustic emissions (TEOAE). Methods The purpose of the research was to evaluate the entire community independently of variables of sex and age. All of the participants were born and lived in a riverside community. After otolaryngologic evaluation, participants were received tympanometry, evaluation of contralateral acoustic reflexes, pure tone audiometry, and recording of TEOAEs with nonlinear click stimulation. Hair samples were collect to measure mercury levels. Results There was no significant correlation between the inhibitory effect of the MOCS, age, and the level of mercury in the hair. Conclusions The pathophysiological effects of chronic exposure may be subtle and nonspecific and can have a long period of latency; therefore, it will be important to monitor the effects of mercury exposure in the central auditory system of the Amazon population over time. Longitudinal studies should be performed to determine whether the inhibitory effect of the MOCS on otoacoustic emissions can be an evaluation method and diagnostic tool in populations exposed to mercury. .


Subject(s)
Humans , Spondylarthritis/epidemiology , Africa South of the Sahara/epidemiology , Arthritis, Psoriatic/epidemiology , Arthritis, Psoriatic/genetics , Arthritis, Psoriatic/virology , Arthritis, Reactive/epidemiology , Arthritis, Reactive/genetics , Arthritis, Reactive/virology , Genetic Predisposition to Disease , HIV Infections/complications , /genetics , Spondylarthritis/diagnosis , Spondylarthritis/genetics , Spondylarthritis/virology , Spondylitis, Ankylosing/epidemiology , Spondylitis, Ankylosing/genetics , Spondylitis, Ankylosing/virology
2.
Arq. neuropsiquiatr ; 64(3b): 872-876, set. 2006. graf, tab
Article in English, Portuguese | LILACS | ID: lil-437166

ABSTRACT

Herein, we report a case of multiple sclerosis in which peripheral and central hearing, were evaluated through early (brainstem), middle and late auditory evoked potentials before and after corticosteroid therapy. Auditory evaluation revealed better performance on all post-treatment tests. In this case, central auditory function tests (behavioral and electrophysiological) identified the location of the impairment (brainstem), which was in agreement with the patient complaint. The speech in noise test and brainstem auditory evoked potentials are definitely appropriate in confirming brainstem lesions.


Relatamos caso de esclerose múltipla em que foi feita avaliação da audição periférica e central utilizando os potenciais evocados auditivos de curta, média e longa latência antes e depois da terapia com corticosteróides. A avaliação auditiva revelou melhor desempenho em todos os testes após o tratamento. Neste caso, os testes que avaliam a função central da audição (comportamental e eletrofisiológico) foram capazes de identificar o local da lesão (tronco encefálico), o que estava de acordo com as queixas do paciente. Os testes de fala com ruído e os potenciais evocados auditivos de curta latência são apropriados para revelar lesões de tronco encefálico.


Subject(s)
Adult , Humans , Male , Audiometry, Pure-Tone , Adrenal Cortex Hormones/therapeutic use , Auditory Perceptual Disorders/etiology , Multiple Sclerosis/complications , Reaction Time/physiology , Auditory Perceptual Disorders/drug therapy , Auditory Perceptual Disorders/physiopathology , Electrophysiology , Multiple Sclerosis/physiopathology
SELECTION OF CITATIONS
SEARCH DETAIL