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8 results
Pattern of Idiopathic Intracranial Hypertension in Indian Population.
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Idiopathic intracranial hypertension: clinical features in Chinese patients.
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OBJECTIVE
To describe the clinical features and visual outcomes of idiopathic intracranial hypertension (IIH) in Chinese patients.
METHODS
We retrospectively reviewed the charts of patients diagnosed with IIH in Taipei Veterans General Hospital from 1981 to 2009. Demographic data, clinical features,
[Retinal pigment epithelium--the point about safety of antimalarial agents].
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The antimalarial agents Chloroquine and Hydroxychloroquine are used for the treatment of inflammatory disorders such as rheumatoid arthritis and lupus erythematosus. The first published reports of retinal toxicity appeared in 1959. Despite a low incidence for low doses and a short period of time, a
A 43-year-old woman on triptorelin presenting with pseudotumor cerebri: a case report.
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BACKGROUND
To the best of our knowledge, this is the first time triptorelin has been reported to cause benign intracranial hypertension.
METHODS
A 43-year-old Caucasian woman who suffered from chronic menorrhagia was started on triptorelin, a gonadotrophin-releasing hormone analogue. Three days
[Shock-induced anterior ischemic optic neuropathy from hemorrhagic anemia].
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A 51-year-old diabetic and overweight male presented to our eye clinic with right-sided impairment of visual acuity and scotoma. A thorough work-up had been carried out at our institute 9 months prior to this event due to left-sided nonarteriitic anterior ischemic optic neuropathy (NAION). Despite
Pseudotumor Cerebri Syndrome with Resolution After Discontinuing High Vitamin A Containing Dietary Supplement: Case Report and Review.
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A 24-year-old non-obese, but slightly overweight, female presented with a two-week history of progressive severe headache associated with two days of blurry vision. Clinical exam was significant for bilateral papilledema and an enlarged blind spot on visual field testing. Contrast enhanced MRI head
Phenotypic expression of Bardet-Biedl syndrome in patients homozygous for the common M390R mutation in the BBS1 gene.
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OBJECTIVE
To characterize the phenotype of Bardet-Biedl syndrome (BBS) patients homozygous for the BBS1 M390R mutation.
METHODS
Three patients [PT1, F, 27 years old (yo) at last examination, 14-year follow-up (F/U) PT2, F, 15-yo PT3, M, 15-yo, both 1-year F/U] underwent eye exams, Goldmann visual
The idiopathic intracranial hypertension treatment trial: clinical profile at baseline.
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OBJECTIVE
To our knowledge, there are no large prospective cohorts of untreated patients with idiopathic intracranial hypertension (IIH) to characterize the disease.
OBJECTIVE
To report the baseline clinical and laboratory features of patients enrolled in the Idiopathic Intracranial Hypertension
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