Title of article
Childhood moyamoya disease accompanying leigh syndrome
Author/Authors
Çullu, Nesat Mugla Sitki Koçman University - Faculty of Medicine - Department of Radiology, Turkey , Karakas, Ekrem Harran University - Faculty of Medicine - Department of Radiology, Turkey , Karakas, Ömer Harran University - Faculty of Medicine - Department of Radiology, Turkey , Deveer, Mehmet Mugla Sitki Koçman University - Faculty of Medicine - Department of Radiology, Turkey , Çalik, Mustafa Harran University - Faculty of Medicine - Department of Pediatric Neurology, Turkey , Boyaci, Fatima Nurefsan Harran University - Faculty of Medicine - Department of Radiology, Turkey
From page
1538
To page
1540
Abstract
Moyamoya disease is a cerebrovasculopathy of unknown etiology during the course of which the main and terminal veins of the internal carotid artery undergo progressive vein occlusion. Leigh syndrome is a mitochondrial encephalomyopathy that occurs due to cytochrome c oxidase deficiency characterized by psychomotor retardation, difficulty in eating, seizures, hypotonia, respiratory disorders and high lactate levels. Many diseases and syndromes have been defined that are associated with Moyamoya disease. To the best of our knowledge, the association of moyamoya disease with Leigh syndrome has not been defined as yet. In this study, the clinical and imaging results of a 3-year old male child displaying the association of Moyamoya disease and Leigh syndrome are presented.
Keywords
Leigh disease , Moyamoya syndrome , Childhood , MRI.
Journal title
Journal of the Pakistan Medical Association (Centre) JPMA
Journal title
Journal of the Pakistan Medical Association (Centre) JPMA
Record number
2652999
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