amblyopia/infarkt

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9 výsledky

Ophthalmologic findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a cross-sectional study.

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OBJECTIVE To determine the ophthalmologic findings, especially the nature of retinal vascular changes, and their clinical significance in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a disease that causes migraine, recurrent strokes, and

Pattern of ocular dominance columns in human striate cortex in strabismic amblyopia.

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Previous experiments in animals have shown that early unilateral eyelid suture, a model of amblyopia induced by cataract, causes shrinkage of ocular dominance columns serving the deprived eye in the striate cortex. It is unknown whether the ocular dominance columns are affected in amblyopia produced

Unilateral retinal hemorrhages in documented cases of child abuse.

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OBJECTIVE To describe the occurrence of unilateral retinal hemorrhages in four cases of documented child abuse, including a case in which retinal hemorrhages were an incidental finding on routine examination. METHODS Case reports. RESULTS Three children, 5 to 17 months of age, with suspected child

Bilateral occlusion associated to steal phenomenon of internal carotid and left subclavian arteries: treatment by angioplasty and stenting.

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OBJECTIVE Treatment of subclavian artery occlusion is still a matter of controversy due to the short- and long-term complications and patency issues. We report an unusual case of combined occlusion of the proximal segment of the left subclavian artery and subclavian steal phenomenon associated with

[Visual search training for a case of homonymous field defect with multiple visual dysfunctions].

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A 72-year-old right handed man developed right homonymous hemianopia without macular sparing, left homonymous lower quadranopia with macular sparing, cerebral amblyopia, cerebral achromatopsia, impaired form vision, and mild right hemispatial neglect, after multiple cerebral infarctions, involving

COL4A1 mutation in Axenfeld-Rieger anomaly with leukoencephalopathy and stroke.

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OBJECTIVE Several hereditary ischemic small-vessel diseases of the brain have been reported during the last decade. Some of them have ophthalmological, mainly retinal, manifestations. Herein, we report on a family affected by vascular leukoencephalopathy and variable abnormalities of the anterior

Pituitary apoplexy manifested by sterile meningitis.

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Pituitary apoplexy is rare and underdiagnosed. It results from either infarction or hemorrhage into an adenoma of the pituitary gland. The clinical presentation comprises a rapid development of impaired consciousness, severe headache, and amblyopia or diplopia. Meningeal irritation signs are

[Unusual retinal anomaly: the double papilla].

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BACKGROUND It is not clear whether doubling of the papilla occurs in connection with congenital ocular malformations or whether there is a double anlage of a real papilla. A double optic nerve close to the globe has never been observed. METHODS A 87-year old woman had high-grade myopia and amblyopia

Cerebral small vessel disease in pseudoxanthoma elasticum: three cases.

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BACKGROUND Cerebral small vessel disease is rarely described in association with pseudoxanthoma elasticum (PXE), a hereditary connective tissue disorder with skin, eye and vascular manifestations. This autosomally inherited elastic tissue disease has been attributed to mutations in the ABCC6 gene

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