O063. Moyamoya disease and headache: case report.

O063. Moyamoya disease and headache: case report. - PDF Download Free
171KB Sizes 2 Downloads 9 Views

Recommend Documents


Development of moyamoya disease in pregnancy and puerperium: case report.
Progressive moyamoya disease in pregnancy and puerperium has not been reported previously. Here, we present a 39-year-old woman who had been found to have moderate stenosis of right middle cerebral artery (MCA) 4 years prior to her pregnancy, finally

Moyamoya disease with neuro-ophthalmic manifestations: a rare case report.
Moyamoya (meaning a hazy puff of smoke) disease (MMD) is a rare, idiopathic, persistent, occlusive cerebrovascular disease involving bilateral progressive stenosis or occlusion of a terminal portion of the internal carotid artery, or a proximal porti

Case Report: A case report of Moyamoya disease in a 36 year old African American woman.
Moyamoya is a rare idiopathic progressive vaso-occlusive disease characterized by irreversible condition of main blood vessels to the brain as they enter into the skull. We present a case of 36 year old African American female presenting to the Out P

A Case of Homocystinuria Misdiagnosed as Moyamoya Disease: A Case Report.
Homocystinuria is a hereditary disease caused by a defect in the enzymes involved in metabolizing methionine. Homocystinuria can influence many systems and may be mistaken for other diseases, including Moyamoya disease. Here, we report the case of a

One sided bypass for bilateral Moyamoya disease, a case report and review of the literatures.
Moyamoya disease (MMD) is a rare condition, where the most appropriate treatment for it is yet to be determined. Surgery remains an important method of choice although it is considered a form of palliative care. The outcome following surgery is very

Moyamoya disease manifested as multiple simultaneous intracerebral hemorrhages: A case report and literature review.
Multiple simultaneous intracerebral hemorrhages (MSIH) caused by Moyamoya disease (MMD) is extremely rare. To date, the clinical manifestations, imaging characteristics and mechanism of MMD-induced MSIH have not yet been elucidated. In order to impro

Variant angina in moyamoya disease--a correlative etiology and different presentation: a case report.
Moyamoya disease is characterized by progressive steno-occlusive changes of the distal internal carotid and developed collateral vasculature, so called 'moyamoya' vessels at the base of the brain. Variant angina is a rare occurrence in patients with