Refranero, de Ismael Moya

Fallbericht: Moya-Moya-Erkrankung

Moyamoya Disease – Case Report. Moyamoya disease is a more common disease in Asian population and well discussed since 1957. Because of the continuously increasing population of people with migration background, this disease is getting a topical subject in European countries. Characterized by occlusion of the distal carotid arteries, it is a progressive disease with a fragile network of basal c...

Clinical and angiographic findings in Moya Moya

PATIENT Female, 40 FINAL DIAGNOSIS: Moya-Moya Disease Symptoms: Blurred vision • headache • lethargy MEDICATION - Clinical Procedure: - Specialty: Neurology. OBJECTIVE Rare disease. BACKGROUND Moya Moya is a cerebrovasculopathy of the terminal internal carotid arteries and the proximal anterior and middle cerebral arteries. It is comparatively more common in Japan compared to Western coun...

Genetic and immunologic analysis on moya-moya.

The genetic and immunologic abnormalities associated with the pathogenesis of moya-moya were assessed in 23, 13 children and 10 adults with angiographically diagnosed moya-moya. In HLA-A, -B, -C stereotyping, an association was found of AW24, BW46, and BW54 with relative risks of 3.83, 6.50, and 3.58 respectively. Natural T cell toxic autoantibody was detected by FACS analysis in sera from five...

Moya - Albiol

Moya Moya Disease: Presenting With Changing Neurological Signs

A 4 yrs old female child was admitted with left hemiparesis and unconsciousness and a short history of neurological impairment, changing neurological signs with progress of the disease and most of relevant laboratory investigations being normal, child underwent MRI and MRA which revealed features of Moya moya disease.