Abstract:
:Moyamoya is a rare disorder that involves steno-occlusive arterial changes of the anterior circulation, along with proliferative development of basal arterial collaterals. It is either idiopathic (called moyamoya disease) or the result of a specific underlying condition such as atherosclerosis, radiation therapy, or sickle cell disease (called moyamoya syndrome or phenomenon). In recent years, numerous insights into and advances in the understanding, evaluation, and management of moyamoya patients have occurred. This article briefly reviews the spectrum of moyamoya conditions and then provides a synopsis of numerous recent investigations that shed light on various aspects of the disease, including its clinical characteristics, natural history, underlying pathology, imaging, surgical techniques, and long-term patient outcome.
journal_name
Neurosurgeryjournal_title
Neurosurgeryauthors
Arias EJ,Derdeyn CP,Dacey RG Jr,Zipfel GJdoi
10.1227/NEU.0000000000000229subject
Has Abstractpub_date
2014-02-01 00:00:00pages
S116-25eissn
0148-396Xissn
1524-4040pii
00006123-201402001-00014journal_volume
74 Suppl 1pub_type
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