Abstract |
Cogan's syndrome is characterized by interstitial keratitis, vestibular impairment and hearing loss, commonly bilateral. Many patients, especially children, experience a delay in proper diagnosis which may delay treatment and thus impact on prognosis of hearing restoration. Less than 10 pediatric cases of Cogan's syndrome have been reported in literature and only five of them were reported with long-term follow-up. We report an extremely rare pediatric case of Cogan's syndrome typical form with long-term follow-up and evaluation of hearing impairment. Cogan's syndrome must be familiar to otorhinolaryngologists, pediatricians and ophthalmologists because early diagnosis and rapid administration of the proper therapy increase the probability of recovering hearing loss.
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Authors | Ioannis Vasileiadis, Roxani Stratoudaki, Efthimios Karakostas |
Journal | International journal of pediatric otorhinolaryngology
(Int J Pediatr Otorhinolaryngol)
Vol. 76
Issue 4
Pg. 601-5
(Apr 2012)
ISSN: 1872-8464 [Electronic] Ireland |
PMID | 22370237
(Publication Type: Case Reports, Journal Article, Review)
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Copyright | Copyright © 2012 Elsevier Ireland Ltd. All rights reserved. |
Chemical References |
- Glucocorticoids
- Prednisolone
|
Topics |
- Child
- Cogan Syndrome
(complications, diagnosis, therapy)
- Female
- Glucocorticoids
(therapeutic use)
- Hearing Loss, Sensorineural
(diagnosis, etiology, therapy)
- Humans
- Prednisolone
(therapeutic use)
- Recovery of Function
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