Results 21 to 30 of about 1,229,635 (199)

Moyamoya Syndrome and Congenital Heart Disease

open access: yesPediatric Neurology Briefs, 1998
The association of moyamoya syndrome and congenital heart disease is described in 5 patients at Children's Hospital, Boston, MA.
J Gordon Millichap
doaj   +2 more sources

A rare cranial disease: Prolactinoma-associated moyamoya syndrome [PDF]

open access: yesUlusal Romatoloji Dergisi
Moyamoya disease is a rare chronic progressive cerebrovascular disease. The etiology of moyamoya disease has not been established yet. If an underlying cause is detected, moyamoya disease is called moyamoya syndrome.
Ayberk Bayramgil   +3 more
doaj   +2 more sources

Down syndrome associated moyamoya may worsen epilepsy control and can benefit from surgical revascularization

open access: yesEpilepsy and Behavior Case Reports, 2019
Objectives: To examine outcome of bilateral extracranial to intracranial (EC-IC) bypass surgeries for a Down syndrome patient with hard-to-treat epilepsy and moyamoya.
Sarah R. Garson   +5 more
doaj   +4 more sources

Moyamoya disease and syndromes: from genetics to clinical management

open access: yesThe Application of Clinical Genetics, 2015
Stéphanie Guey,1,3 Elisabeth Tournier-Lasserve,1,2 Dominique Hervé,1,3 Manoelle Kossorotoff4 1Inserm UMR-S1161, Université Paris 7 Denis Diderot, Sorbonne Paris Cité, Paris, France; 2AP-HP, Groupe hospitalier Lariboisiè ...
Guey S   +3 more
doaj   +1 more source

Moyamoya angiopathy in a case of Klinefelter syndrome. [PDF]

open access: yes, 2021
20.500.12530/87852Moyamoya angiopathy, a rare cerebrovascular condition, can be primary (moyamoya disease) or secondary (moyamoya syndrome). Genetic factors, such as the ring finger protein 213 (RNF213), have been associated with moyamoya disease ...
Ray, Adrija   +4 more
core   +1 more source

Case Report: A Case of Moyamoya Syndrome Associated With Multiple Endocrine Neoplasia Type 2A

open access: yesFrontiers in Endocrinology, 2021
To the best of our knowledge, we report a case of MEN2A complicated by moyamoya syndrome. A 52-year-old woman presented with vertigo. Magnetic resonance angiography (MRA) revealed bilateral supraclinoid stenosis of the internal carotid artery and ...
Fumihiro Matano   +7 more
doaj   +1 more source

Moyamoya Syndrome: A Window of Moyamoya Disease

open access: yesJournal of Korean Neurosurgical Society, 2015
Moyamoya-like vasculopathy develops in association with various systemic diseases and conditions, which is termed moyamoya syndrome. Relatively common diseases and conditions are related to moyamoya syndrome, including neurofibromatosis type 1, Down syndrome, thyroid disease, and cranial irradiation.
Phi, Ji Hoon   +3 more
openaire   +2 more sources

Abstract Number ‐ 250: Case Series of Moyamoya Patients Diagnosed on Hyperacute Imaging

open access: yesStroke: Vascular and Interventional Neurology, 2023
Introduction Moyamoya disease is the idiopathic bilateral progressive stenosis of the anterior circulation arteries at the skull base, followed by the compensatory formation and proliferation of collateral small vessel arteries typically in the ...
Christina Xia   +2 more
doaj   +1 more source

Co-occurrence of Moyamoya syndrome and Kartagener syndrome caused by the mutation of DNAH5 and DNAH11: a case report

open access: yesBMC Neurology, 2020
Background Kartagener syndrome is an autosomal recessive inherited disorder of primary ciliary dyskinesia. Moyamoya syndrome refers to a moyamoya angiopathy associated with other neurological and/or extra-neurological symptoms, or due to a well ...
Lili Zhang   +4 more
doaj   +1 more source

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