Title of article
Long-term subclinical severe hyperCKemia associated with a rare VPS13A gene mutation in an Iranian patient: Case report
Author/Authors
Hadei ، Jalaleddin Department of Neurology - Shariati Hospital - Tehran University of Medical Sciences , Ghaderi-Yazdi ، Bardiya Department of Neurology - Shariati Hospital - Tehran University of Medical Sciences , Nafissi ، Shahriar Department of Neurology - Shariati Hospital, Iran Neuromuscular Research Center - Tehran University of Medical Sciences
From page
86
To page
88
Abstract
Cerebellar arteriovenous malformations (CAVMs) have increased probabilities of rupture and bleeding compared with arteriovenous malformations (AVMs) in other locations of the brain. The treatment of CAVMs includes craniotomy, endovascular treatment (EVT), radiotherapy, or a combination of multiple methods. EVT has been used in an increasing number of CAVM cases and is difficult, as the angioarchitecture of CAVMs is complex, consisting of the feeding artery, nidus, draining vein, and aneurysm on the feeding artery and in the nidus.
Keywords
VPS13A Protein Human , Genetic Testing , Chorea , Acanthocytosis , Neuromuscular Disease , Creatine Kinase , Movement Disorders
Journal title
current journal of neurology
Journal title
current journal of neurology
Record number
2779597
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