Studies on children with deafness due to meningitis.

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منابع مشابه

Evaluation of Aseptic Meningitis Following Measles-Mumps-Rubella Vaccine in Children Admitted due to Febrile Convulsion

Background Febrile convulsion (FC) is the most common neurological problem in children which can occur in 2 to 5% of this population. The most important issue is to identify the cause of fever and rule out bacterial meningitis. The purpose of this study was to evaluate the association of aseptic meningitis due to Measles-Mumps-Rubella (MMR) vaccine in admitted children with febrile convulsion. ...

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Deafness after bacterial meningitis.

Seventeen children with previous bacterial meningitis and 17 sib controls were examined clinically and otoscopically. They were also tested with air-conduction and bone-conduction audiometry and evaluated by tympanometry. There were no major neurological abnormalities and few otoscopical signs of ear disease. 21% of the ears showed abnormalities on air-conduction audiometry but all were normal ...

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Deafness due to haemorrhagic labyrinthitis and a review of relapses in Streptococcus suis meningitis.

Deafness is a common and often permanent neurological sequel of Streptococcus (S.) suis meningitis. Suppurative labyrinthitis, rather than direct auditory nerve infection, has been found to be the site responsible for deafness. Neuroimaging is important to localise the site involved in hearing loss and to assess the feasibility of a cochlear implantation. S. suis is very sensitive to penicillin...

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Children\'s Deafness

This is an article about children's deafness, it's ethiology, diagnosis, treatment, and educa­tional treatment. Here I have given a brief account about the deafness itself and it's in­dividual and social complications, also it's im­pression on the psychological well baing of the child. Then I have discussed, rather in detail, the ethiology of .children's deafness and I have given some statistic...

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Cochlear implantation in children with congenital X-linked deafness due to novel mutations in POU3F4 gene.

OBJECTIVES We report novel mutations in the POU3F4 gene resulting in congenital X-linked deafness DFN3, and describe the results of cochlear implantation in 4 boys (3 siblings) followed for an average of 3.5 years. METHODS The diagnosis of DFN3 was made in infant boys on the basis of the radiologic criteria of an underdeveloped modiolus, a wide cochlear fossette, and the presence of all cochl...

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ژورنال

عنوان ژورنال: AUDIOLOGY JAPAN

سال: 1986

ISSN: 1883-7301,0303-8106

DOI: 10.4295/audiology.29.501