Neurophysiologic tests screening cognitive impairment in idiopathic intracranial hypertension patients
نویسندگان
چکیده
منابع مشابه
Idiopathic intracranial hypertension in pediatric patients
PURPOSE To evaluate retrospectively the features, treatment, and outcome of idiopathic intracranial hypertension (IIH) in children. METHODS Nine patients, 15 years and younger, diagnosed with IIH. Inclusion criteria were papilledema, normal brain computer tomography or magnetic resonance imaging, cerebrospinal fluid pressure greater than 250 mm H(2)O, normal cerebrospinal fluid content, and a...
متن کاملIdiopathic intracranial hypertension.
Idiopathic intracranial hypertension is common in obese women and can lead to significant visual impairment. First described more than 100 years ago, the cause of the disorder remains unknown. Despite a multitude of proposed links, the aetiology has never been established. Impairment of cerebrospinal-fluid reabsorption is the most likely underlying pathophysiological cause of the raised pressur...
متن کاملIdiopathic intracranial hypertension.
Although the cause of IIH remains obscure, loss of visual function is common, and patients may progress to blindness. Diagnosis should adhere to the modified Dandy criteria. Recent case-control studies cast doubt on the validity of many frequently cited conditions associated with IIH. Valid associations include obesity, recent weight gain, female sex, vitamin A intoxication, and steroid withdra...
متن کاملIdiopathic Intracranial Hypertension (IIH).
The first report of Idiopathic Intracranial Hypertension (IIH) was by Quinche in 1893. Throughout history it has had many names. When I was a child growing up, before we had antibiotic therapy, middle ear infections occasionally would trigger intracranial inflammation and the disease was called Otitic Hydrocephalus. Then it was called Benign Intracranial Hypertension which we now know is far fr...
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ژورنال
عنوان ژورنال: The Egyptian Journal of Neurology, Psychiatry and Neurosurgery
سال: 2018
ISSN: 1687-8329
DOI: 10.1186/s41983-018-0010-6