Geometry.Net - Health_Conditions: Moyamoya Disease

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Hemidystonia and Hemichoreoathetosis as an Initial Manifestation of moyamoya diseaseAuthor Information Chul Hyoung Lyoo, MD; Seung Hun Oh, MD; JinYang Joo, MD
http://archneur.ama-assn.org/issues/v57n10/abs/nob00014.html

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Moyamoya Disease
only. moyamoya disease,, Print this article, a moyamoya disease, Fig.1 a, b. Lateral and AP right carotid angiogram. The supraclinoidal
http://www.amershamhealth.com/medcyclopaedia/Volume VI 1/MOYAMOYA DISEASE.asp

Extractions: *For Medical Professionals only, registration required Moyamoya disease, a progressive occlusive disease of the basal cerebral vessels forming the circle of Willis, of unknown aetiology. The clinical presentation is characterized by repeated ischaemic episodes in children and adolescents; the severity of the neurological deficits depends on the rapidity of progression, and the extent of the disease. Progressive occlusion of the distal portion of the internal carotid arteries and of the proximal segments of the middle cerebral arteries is the angiographic hallmark of the disease together with a peculiar collateral circulation that involves meningeal vessels with transdural anastomosis and penetrating vessels of the basal ganglia. Hypertrophy of lenticulostriate arteries and thalamoperforating arteries leads to the characteristic appearance first described in the Japanese literature as the "puff of smoke" or Moyamoya. Although MR can show the infarcted areas of the brain the diagnostic modality of choice is cerebral angiography ( Fig.1
Moyamoya Disease
by only one click For Medical Professionals only. moyamoya disease,,Print this article, meaning 'puff of smoke' in Japanese, a
http://www.amershamhealth.com/medcyclopaedia/Volume VII/MOYAMOYA DISEASE.asp

Extractions: *For Medical Professionals only, registration required Moyamoya disease, meaning 'puff of smoke' in Japanese, a term used to describe the appearance of multiple collateral vessels, usually lenticulostriate and thalamostriate vessels, seen on cerebral angiography in patients with a vasculopathy characterised by progressive stenosis of the distal internal carotid arteries and the major intracranial arteries. The posterior circulation is less commonly involved. Though the condition is seen in adults 50% of reported cases of moya-moya syndrome occur in patients under 10 years, with 70% under 20% years. Patients usually present with transient ischaemic attacks, headache or seizures. Familial cases of the condition have been reported in Japan. The condition may also be seen in patients with phakomatosis, such as neurofibromatosis type 1 and tuberous sclerosis Downs syndrome , following radiation therapy, polyarteritis nodosa and Takayasus arteritis , and sickle cell diseases . When no cause is found the condition is known as moya-moya disease. The definitive diagnosis is made on cerebral angiography where stenoses in the distal internal carotid and intracranial circulation are seen in association with multiple small collateral vessels in the region of the thalamostriate and lenticulostriate arteries.
Nature Publishing Group
Case Report. moyamoya disease associated with renovascular disease in a young AfricanBrazilianpatient. Keywords. moyamoya disease; renovascular hypertension.
http://www.nature.com/cgi-taf/DynaPage.taf?file=/jhh/journal/v15/n7/abs/1001207a
Health Library - Moyamoya Disease
moyamoya disease. None. General Discussion. moyamoya disease is a progressivedisease that affects the blood vessels in the brain (cerebrovascular).
http://www.laurushealth.com/library/healthguide/illnessconditions/topic.asp?hwid
1Up Health Moyamoya Disease - Rare Disorders
moyamoya disease . Read detailed information about moyamoya disease . Search 1Up Health.1Up Health Diseases Conditions Rare Disorders moyamoya disease.
http://www.1uphealth.com/medical/disease/rare-disorder-disease/moyamoya-disease.
1Up Health > Health Links Directory > Conditions And Diseases: Rare Disorders: M
Sites. Chorus Notecard Document A definition of moyamoya disease alongwith clinical and radiographic finding. EMedicine MMD An
http://www.1uphealth.com/links/rare-disorders-moyamoya.html
MOYAMOYA DISEASE : A Mystery Of Inherited Human Afflication. Can Mendelian Genom
moyamoya disease A mystery of inherited human afflication. Can Mendeliangenomics solve the puzzle? Find out. 1. moyamoya disease.
http://databank.oxydex.com/compendium_bibliographium/awaiting_human_genome/MOYAM

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Cardiovascular Diseases
moyamoya disease MoyaMoya Syndrome - Neurology Web Forum (US); AboutMoya-Moya and Surgery - Columbia Univ Coll (US); Re Moyamoya
http://www.mic.ki.se/Diseases/c14.html
Moyamoya Disease Information Page Diseases Database
moyamoya disease Information Page. 2 synonyms or equivalents were found.moyamoya disease aka/or MoyaMoya disease related topics
http://www.diseasesdatabase.com/sieve/item1.asp?glngUserChoice=8384
Moyamoya Disease - General Practice Notebook
moyamoya disease. moyamoya disease may present with stroke in childrenand young adults. The cause of the disease is unknown. It
http://www.gpnotebook.co.uk/cache/939917343.htm

Extractions: Moyamoya disease Moyamoya disease may present with stroke in children and young adults. The cause of the disease is unknown. It was first described in 1963; early reports were predominantly in Japanese patients although later reports include non-Japanese. It arises in the presence of bilateral occlusion of the carotid arteries resulting in the development of an extensive fine network of collateral arteries and arterioles at the base of the brain - collaterals resemble a puff of smoke. Children typically present with sudden ischaemic strokes whilst young adults more commonly present with a sub-arachnoid haemorrhage. There is no specific treatment but surgical revascularisation may be tried.
Advanced Respiratory - Airway Clearance Indications Of Moyamoya Disease
Airway Clearance Indications of moyamoya disease moyamoya disease is acerebrovascular disease which, as it progresses, is characterized
http://www.abivest.com/conditions/factsheets/moyamoya.asp?printVersion=1&gs=pati
NORD - National Organization For Rare Disorders, Inc.
moyamoya disease. To purchase fulltext report ($7.50) View Cart/Checkout.Copyright 1989, 1996 Synonyms of moyamoya disease Moya-moya Disease.
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Moyamoya Dise
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moyamoya disease. moyamoya disease causes blood vessels leading to the brain tonarrow and close. It is rare and can occur during childhood or adulthood.
http://cgi.stanford.edu/~amlin/cgi-bin/find_specialist?action=get_description&di
Lasion Europe-Table Of Contents
MRA OF OCCLUSIVE CEREBRAL ANGIOPATHIES (moyamoya disease). moyamoya diseasegeneral considerations moyamoya disease imaging strategies
http://sme.belgium.eu.net/lasion/trmri2.htm

Extractions: APPLIED MR NEURO-ANGIOGRAPHY AUTHORS' LIST Authors' list ACKNOWLEDGEMENTS Acknowledgements INTRODUCTION Introduction PART I: THEORETICAL AND TECHNICAL CONSIDERATIONS MR signal of static blood and hemorrhage EFFECTS OF SPIN MOTION ON THE MR SIGNAL: BASIC FLOW PHENOMENA TIME-OF-FLIGHT EFFECTS In-flow effects: flow-related enhancement
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http://medicine.chungbuk.ac.kr/~march/self/moya/moya.htm

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Health Library - Moyamoya Disease
Saint Luke's Health System eLibrary. moyamoya disease. moyamoya disease is a progressivedisease that affects the blood vessels in the brain (cerebrovascular).
http://hvelink.saint-lukes.org/library/healthguide/IllnessConditions/topic.asp?h
ICP Monitors
moyamoya disease. Historical. Defintion. Etiology. moyamoya disease, seenin Japanese population, young and old. Etiology of disease remains unknown.
http://www.ucch.org/sections/neurosurg/NeuroReview/05-Vascular/MoyaMoya.html

Extractions: Moyamoya Disease Historical Defintion . A chronic occlusive cerebrovascular disease characterized by progressive stenosis of the proximal internal carotid artery and its branches, with concommitant enlargement of tiny subsidiary and proximal penetrating arteries at the base of the brain to form the characteristic moyamoya vessels. (From Pediatric Neurosurgery , p. 518, Scott, et al). described this condition affecting Japanese families in 1969. Th e hallmark of the condition, referring to the angiographic appearance of the dilated collateral vessels, was called moyamoya or "puff of smoke". Etiology seen in Jap anese population, young and old. Etiology of disease remains unknown. nonspecific angiographic appearance seen with: meningitis (tuberculous and leptospirosis) a therosclerosis radiation therapy sickle cell anemia (and other inherited disorders such as NF) (Moyamoya seen on MARS Pathology Moyamoya vessels are basically markedly dilated intracerebral perforating arteries and arterioles without abnormal histology . Microaneurysms can be present. Stenotic/occluded vessels show nonspecific changes such as intimal thickening and hyperplasia, and irregularities of the internal elastic lamina.
ÄÊÁ êáé Stroke - Moyamoya
Annual report of 1978 of the Research Committee on Spontaneous Occlusion of theCircle of Willis (moyamoya disease) of the Ministry of Health and Welfare
http://users.med.auth.gr/~georgak/sel_top/sickle/moyamoya.html

Extractions: Ç ÍÏÓÏÓ moyamoya Ðñéí ðñï÷ùñÞóïõìå óôçí åñìçíåßá ôùí åíäïêñáíéáêþí áéìïññáãéþí óå áóèåíåßò ìå ÄÊÁ åßíáé áíáãêáßï íá áíáöåñèïýìå óôç íüóï moyamoya, áöïý öáßíåôáé ðùò ðïëý óõ÷íÜ ïé áããåéáêÝò âëÜâåò ôùí áóèåíþí áõôþí äåí åßíáé ôßðïôå Üëëï áðü ìéá ðåñßðôùóç öáéíüìåíïõ moyamoya. Moyamoya åßíáé ìéá ãéáðùíÝæéêç ëÝîç ðïõ ìåôáöñÜæåôáé ôïëýðç êáðíïý êáé ôç ÷ñçóéìïðïßçóå ï Suzuki íüóïò moyamoya öáéíüìåíï moyamoya. ¼ôáí ïé ÷áñáêôçñéóôéêÝò áõôÝò áããåéáêÝò áëëïéþóåéò áíåõñßóêïíôáé åôåñüðëåõñá êáé éó÷ýåé êáé ôï êñéôÞñéï 3, ôüôå ç äéÜãíùóç ìðïñåß íá ôåèåß ùò ðéèáíÞ (probable).
Moya Moya Syndrome: Homefield Info
.Moya Moya. moyamoya disease is a progressive cerebrovascular occlusive disease thatoccurs in children. The etiology is unknown. moyamoya disease.
http://www.swis.net/midgley/moya1.htm

Extractions: for the Web minder robot Moyamoya disease is a progressive cerebrovascular occlusive disease that occurs in children. The etiology is unknown. It is rare in Exeter Moyamoya disease affects the cerbrovascular circulation by increasingly narrowing and in some cases eventually occluding the terminal portion of the internal carotid artery. The age of onset appears to dictate the manifestations. For example, children may experience seizures or involuntary movements and even exhibit signs of mental retardation. In young patients, moyamoya disease is usually associated with headaches, speech difficulties, paralytic episodes involving the feet, legs or upper extremeties, hemorrhage and anemia. In adults, disturbance of consciousness or subarachnoid hemorrhage is prominent. The patient may have syncopal episodes. In addition, these visual abnormalities may occur alone or in combination, hemianopia, diplopia, bilaterally diminished visual acuity, and the inability to recognize objects: papilledema may indicate subarachnoid or cerebral hemorrhage. Moyamoya disease is idiopathic. In a few patients, it has been attributed to an autosomal recessive trait. Studies have implicated oral contraceptives in a small number of female patients, but this has not been substantiated. Pregnancy may also be a factor.

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