Open AccessEpidemiology, diagnosis and treatment of moyamoya disease (Review)
Author(s) -
Hui Zhang,
Lijian Zheng,
Lei Feng
Publication year - 2019
Publication title -
experimental and therapeutic medicine
Language(s) - English
Resource type - Journals
eISSN - 1792-1015
pISSN - 1792-0981
DOI - 10.3892/etm.2019.7198
Subject(s) - moyamoya disease , medicine , disease , revascularization , stroke (engine) , epidemiology , occlusion , cardiology , epilepsy , intensive care medicine , myocardial infarction , psychiatry , mechanical engineering , engineering
Moyamoya disease (MMD) is a type of chronic cerebrovascular occlusion disease, which frequently occurs in East Asian populations, including pediatric and adult patients, and may lead to ischemic or hemorrhagic stroke, headache, epilepsy or transient ischemic attack. To date, the underlying mechanisms of MMD have remained to be fully elucidated, but certain studies have indicated that genetic factors may be an important component of its development. Cerebral angiography is the best approach for diagnosing MMD. However, with technological advances, non-invasive techniques are increasingly used to accurately evaluate MMD. MMD is commonly treated via surgery, and an increasing number of patients are benefitting from the intra- and extra-cranial revascularization. The present article provides a comprehensive review of MMD on the basis of previous research.