منابع مشابه
[Sensorineural hearing loss evolution in Vogt-Koyanagi-Harada syndrome].
Vogt-Koyanagi-Harada syndrome is an autoimmune multisystem disease, characterized by the association of ocular inflammatory manifestations (uveitis and retinal detachment) and extraocular lesions such as meningismus and tegumentary or auditory findings. We report the case of a Hispanic woman with this syndrome.
متن کاملVogt-Koyanagi-Harada disease: a disorder unfamiliar to dermatologists.
Vogt-Koyanagi-Harada disease is a rare condition that is characterized by bilateral uveitis, meningitis, auditory symptoms, and skin disorders such as vitiligo, poliosis, and alopecia. This report aims to draw attention to a condition that is widely discussed in the literature yet unfamiliar to dermatologists. We present the case of a 37-year-old man from Bolivia who was seen in the emergency d...
متن کاملHeadache, red eyes, blurred vision and hearing loss. Diagnosis: Vogt-Koyanagi-Harada syndrome.
متن کامل
Speech Processing Disorder in Neural Hearing Loss
Deficits in central auditory processing may occur in a variety of clinical conditions including traumatic brain injury, neurodegenerative disease, auditory neuropathy/dyssynchrony syndrome, neurological disorders associated with aging, and aphasia. Deficits in central auditory processing of a more subtle nature have also been studied extensively in neurodevelopmental disorders in children with ...
متن کاملVogt-koyanagi-harada Syndrome
CASE PRESENTATION A 20 year old Asian male was referred with the complaint of decreased vision in both eyes for a year. His past medical and surgical histories were unremarkable. His family history revealed thyroid disease in his mother. Review of systems were remarkable for alopecia and headache at the time when his eye problems began. The first eye exam from his referring ophthalmologist reve...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: AUDIOLOGY JAPAN
سال: 1990
ISSN: 1883-7301,0303-8106
DOI: 10.4295/audiology.33.603