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Moyamoya Disease: more detail

Moyamoya Disease Update
Moyamoya Disease
The Official Parent's Sourcebook on Moyamoya Disease: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-11
Moyamoya Disease by Jiro Suzuki, 1986-06
Moyamoya disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Dawn, MS, CGC Cardeiro, 2005
Moyamoya disease and aortic coarctation in a patient with common brachiocephalic trunk/Moyamoya hastaligi ve aort koarktasyonunun eslik bir brakiyosefalik ... of Cardiology (Anadolu Kardiyoloji Dergisi) by Kadir Babaoglu, Tevfik Demir, et all 2007-03-01
Nursing issues in caring for children with moyamoya vasculopathy and their families.(Disease/Disorder overview): An article from: Journal of Neuroscience Nursing by Selina Y.C. Hune, Gabrielle A. deVeber, et all 2007-02-01
The Official Parent's Sourcebook on Moyamoya Disease A Revised and Updated Directory for the Internet Age by Icon Health Publications, 1980
Tracking recovery in a case of Moyamoya-induced dysarthria.(Report): An article from: Journal of Medical Speech - Language Pathology by Cheryl L. Giddens, Glenda J. Ochsner, 2009-09-01
Moyamoya: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by David, MD Greenberg, 2005

lists with details

Clinical And Experimental Pathology Of Moyamoya Disease
Conclusions The etiology of moyamoya disease may involve allergic angiitis. moyamoya disease, also called abnormal vascular network at the base of the
http://www.cmj.org/information/full.asp?id=1402
Clinical And Experimental Pathology Of Moyamoya Disease
Conclusions The etiology of moyamoya disease may involve allergic angiitis.A possible mechanism is that proximal portions of the circle of Willis first
http://www.cmj.org/information/abstract.asp?id=1402
Diagnosis Of Moyamoya Disease With Transcranial Doppler Sonography: Correlation
Although the diagnosis of moyamoya disease may be confirmed by digital Consecutive patients ( 15 years of age) diagnosed with moyamoya disease by a
http://jon.sagepub.com/cgi/content/abstract/14/4/319

Extractions: This Article Full Text (PDF) References Alert me when this article is cited ... Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Reprints and Permissions PubMed PubMed Citation Articles by Lee, Y.-S. Articles by Roh, J.-K. Yong-Seok Lee, MD, PhD Department of Neurology and Clinical Research Institute, Seoul Municipal Boramae Hospital, Seoul, Korea. Keun-Hwa Jung, MD Seoul National University Hospital, Seoul, Korea. Jae-Kyu Roh, MD, PhD Seoul National University Hospital, Seoul, Korea., Background and Purpose. Although the diagnosis of moyamoya disease may be confirmed by digital subtraction angiography, recent
Neurosurgery - Abstract: Volume 20(1) January 1987 P 33-5 Moyamoya Disease Prese
moyamoya disease presenting as intracerebral hemorrhage during pregnancy case The authors present a case of moyamoya disease associated with pregnancy.
http://www.neurosurgery-online.com/pt/re/neurosurg/abstract.00006123-198701000-0
Neurosurgery - Abstract: Volume 54(4) April 2004 P 840-846 Moyamoya Disease Amon
moyamoya disease among Young Patients Its Aggressive Clinical Course and OBJECTIVE The prognosis for moyamoya disease (MMD) among young patients is
http://www.neurosurgery-online.com/pt/re/neurosurg/abstract.00006123-200404000-0

Extractions: OBJECTIVE: The prognosis for moyamoya disease (MMD) among young patients is known to be worse than that among older patients. The aim of this study was to investigate the clinical features and treatment outcomes of young patients with MMD. METHODS: A total of 204 patients with MMD who underwent encephaloduroarteriosynangiosis, with or without bifrontal encephalogaleosynangiosis, were categorized into three groups according to their ages at the time of surgery, i.e., Group A (n = 23, 6 yr of age). For each group, patterns of presentation and the occurrence of subsequent preoperative or surgery-related infarctions were assessed. Clinical outcomes and postoperative hemodynamic status were analyzed. RESULTS: At initial presentation, infarctions were significantly more frequent in Group A (87%) and Group B (58%) than in Group C (46%). Subsequent preoperative infarctions occurred significantly more frequently in Group A (39%) than in Group B (6%) or Group C (0.8%). The median interval between the onset of symptoms and a subsequent preoperative infarction was 3 months (range, 1-14 mo). No significant difference in the rates of surgery-related infarctions among the three groups was observed. The rate of favorable clinical outcomes was significantly lower in Group A (58%) than in Group B (84%) or Group C (86%), although the rates of postoperative hemodynamic improvements were similar among the groups. The poor clinical outcomes for Group A were caused mainly by preoperative infarctions.
Moyamoya Disease
Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes
http://www.amershamhealth.com/medcyclopaedia/medical/Volume VI 1/MOYAMOYA DISEAS

Extractions: financial services our commitment our company Search Medcyclopaedia for: Search marked text (mark text before you click) Browse entry words starting with: A B C D ... amershamhealth.com 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
Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes
http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/MOYAMOYA DISEASE

Extractions: financial services our commitment our company Search Medcyclopaedia for: Search marked text (mark text before you click) Browse entry words starting with: A B C D ... amershamhealth.com 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. MRI may make the diagnosis though the number of collaterals and the extent of disease may be underestimated. Areas of focal infarction both acute, subacute and chronic, may be evident on both CT and MRI. After intravenous contrast administration intense enhancement may be seen in the deep grey nuclei either from infarction or enhancement of the collateral vessels. Enlargement of the perivascular spaces (VirchowRobin) spaces with enhancement of the collateral vessels within them may also be seen on MRI. Prognosis is variable and may be worse if there is a pre-existing condition. The idiopathic form may not progress. The creation of external carotid to internal carotid anastamoses has been used to bypass the strictured areas.
Moya Moya Disease - Wikipedia, The Free Encyclopedia
moyamoya disease is an extremely rare disorder in most parts of the world except in The pathogenesis of moyamoya disease is unknown. moyamoya disease is
http://en.wikipedia.org/wiki/Moya_Moya_Disease

Extractions: You did it! Over US$240,000 was donated in the 21 day fund drive. Thank you for your generosity! You are still welcome to make a donation or purchase Wikimedia merchandise Moyamoya disease is an extremely rare disorder in most parts of the world except in Japan. The pathogenesis of Moyamoya disease is unknown. Moyamoya disease is characterized by progressive intracranial vascular stenoses of the circle of Willis, resulting in successive ischemic events. Hemmorhagic events can also occur. The condition leads to irreversible blockage of the main blood vessels-the carotid arteries- to the brain as they enter into the skull. It is a disease that tends to affect children and adults in the third to fourth decades of life. In children it tends to cause strokes or seizures. In adults it tends to cause bleeding or strokes. The clinical features are cerebral ischaemia (strokes), recurrent transient ischaemic attacks (TIA's or "mini strokes"), sensorimotor paralysis (numbness in the extremeties), convulsions and/or migraine -like headaches The process of blockage (vascular occlusion) once it begins tends to continue despite any known medical management unless treated with surgery. The repeated strokes can lead to severe functional impairment or even death so it is important to recognize these lesions and treat them early on. Without treatment, there is progressive deterioration of neurologic function and re-hemorrhage.
Blackwell Synergy - Cookie Absent
moyamoya disease is a condition that results from bilateral stenosis or Surgical treatment for moyamoya disease is often complicated by cerebral
http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9592.2005.01576.x

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Moyamoya Syndrome In Children With Alagille Syndrome: Additional Evidence Of A V
collateral route of blood flow.10 The etiology of moyamoya disease is unknown.Pathologically, the cerebral vessels in moyamoya disease are abnormal and
http://pediatrics.aappublications.org/cgi/content/full/103/2/505

Extractions: This Article Extract Full Text (PDF) P ... Citation Map Services E-mail this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Woolfenden, A. R. Articles by Farrell, K. Related Collections Moyamoya Syndrome in Children With Alagille Syndrome: Additional Evidence of a Vasculopathy Alagille syndrome (arteriohepatic dysplasia) is a congenital disorder that can affect the liver, heart, eye, skeleton, and facial appearance. It is associated with bile duct paucity and is an important cause of neonatal jaundice and cholestasis in older children. The most common cardiac malformation associated with Alagille syndrome is peripheral pulmonary stenosis. This syndrome has an autosomal dominant inheritance with variable penetrance, although sporadic cases are common.
IngentaConnect Temporal Profile Of Angiographical Stages Of Moyamoya Disease: Wh
Temporal profile of angiographical stages of moyamoya disease When does Moyamoya To elucidate the initiation of moyamoya disease, we analyzed the
http://www.ingentaconnect.com/content/maney/nres/2003/00000025/00000004/art00015

Extractions: For Researchers For Librarians Authors: Ishii K. ; Isono M.; Kobayashi H.; Kamida T. Source: Neurological Research , Volume 25, Number 4, June 2003, pp. 405-410(6) Publisher: Maney Publishing View Table of Contents full text options Abstract: Keywords: MOYAMOYA DISEASE CEREBRAL ANGIOGRAPHY MAGNETIC RESONANCE IMAGING Document Type: Research article DOI: Affiliations: Department of Neurosurgery, Oita Medical University, Oita, Japan The full text article is available for purchase $38.00 plus tax
IngentaConnect Moyamoya Disease Complicated By Life-threatening Epistaxis: First
Emergency angiography revealed advanced moyamoya disease, with occlusion of bothinternal Conclusion Epistaxis complicating moyamoya disease is rare,
http://www.ingentaconnect.com/content/tandf/soto/2004/00000124/00000002/art00017

Extractions: For Researchers For Librarians Authors: Albrecht Hochmuth ; Ulrich Gollner ; Carsten Christof Boedeker ; Joachim Klisch Source: Acta Oto-Laryngologica , Volume 124, Number 2, March 2004, pp. 206-209(4) Publisher: Taylor and Francis Ltd View Table of Contents full text options Free trial available! Abstract: Keywords: angiography diagnostic imaging embolization endovascular therapy ... treatment outcome Document Type: Research article DOI: Affiliations: Department of Head and Neck Surgery University of Freiburg Freiburg Germany The full text article is available for purchase $38.12 plus tax
Select A Medical Service | Cerebrovascular Disease Center
In patients with moyamoya disease, the enlargement of some of the vessels moyamoya disease is most common in the Asian population and the term moyamoya
http://www.lahey.org/Medical/CerebroVascular/MoyamoyaDisease.asp

Extractions: - - Main Menu Options - - Lahey Homepage Patient Resource Center Select a Medical Service Find a Primary Care Physician Health Information Refer a Patient For Health Care Professionals Careers at Lahey About Lahey Specialty Services: About Our Services: Further Information: Health Encyclopedia Becoming a Lahey Patient Schedule an initial consult with a Lahey primary care physician or specialist. About Lahey Learn about our organization, discover our history, and meet our leaders. Discover what's new at Lahey through our press releases and latest publications. Home Select a Medical Service Cerebrovascular Disease Center - - Quick Browse Disorders Treated - - Arteriovenous Fistula Arteriovenous Malformation (AVM) Carotid Artery Disease Cavernous Angioma Cerebral Aneurysm Intracranial Vascular Disease Ischemic Stroke Moyamoya Disease Spinal Vascular Malformations Stroke Subarachnoid Hemorrhage Vascular Compression Syndromes Vascular Malformations What is moyamoya disease?
Moyamoya Disease Presenting With Singing Induced Chorea -- HAN Et Al. 69 (6): 83
moyamoya disease is a relatively uncommon, chronic cerebral vasculopathy of Chorea is not unusual in moyamoya disease. However, the causes of chorea are
http://www.jnnp.com/cgi/content/full/69/6/833

Extractions: Vol Page [Advanced] This Article Extract Submit a response Alert me when this article is cited Alert me when eLetters are posted ... Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by HAN, S-H Articles by CHUNG, S-Y Related Collections Other Neurology J Neurol Neurosurg Psychiatry 833-834 ( December ) Moyamoya disease is a relatively uncommon, chronic cerebral vasculopathy of unknown aetiology that is characterised by unilateral or bilateral stenosis or occlusion of the proximal portion of the carotid arteries, together with an abnormal vascular network
Moyamoya Disease Presenting As Valsalva Related Partial Seizures -- ROBERTSON Et
moyamoya disease is an idiopathic cerebrovascular disease causing occlusion ofthe terminal Cerebral infarction due to moyamoya disease in young adults.
http://www.jnnp.com/cgi/content/full/66/1/111

Extractions: Vol Page [Advanced] This Article Extract Full Text (PDF) Submit a response ... Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by ROBERTSON, N P Articles by KIRKPATRICK, P Related Collections Neuropathology Other Neurology J Neurol Neurosurg Psychiatry 111 ( January ) A female patient presented aged 13 with occasional stereotypic episodes of dizziness followed by jerking of her right leg spreading rapidly to her right arm over a few minutes without loss of consciousness. An EEG disclosed a right sided slow wave disturbance which increased with overbreathing and cranial CT was normal. Her seizures resolved on a small dose of carbamazepine.
Radiology In Ped Emerg Med, Vol 3, Case 9
The classic puff of smoke pattern seen in moyamoya disease was not moyamoya disease is a disease of the large cerebral vessels that results in a
http://www.hawaii.edu/medicine/pediatrics/pemxray/v3c09.html

Extractions: L = Lateral ventricles. The anterior horns and the posterior horns are shown in this diagram. 3 = Third ventricle. CC = Corpus callosum. C = Caudate nucleus. P = Putamen G = Globus Pallidus. The putamen and globus pallidus together form the lenticular (lentiform) nucleus. T = Thalamus Arrows = Internal Capsule [anterior limb, posterior limb, genu (bend)]. O = Optic radiations. A = Auditory radiations. The corticospinal tract originates from the motor strip of the cerebral cortex. The fibers collect as they traverse through the posterior limb of internal capsule. The tract largely crosses the midline in the decussation of the pyramids. Fibers exit the spinal cord at their respective levels. View our patient's CT scan. T1 (left image) and T2 (right image) weighted axial images are shown (different levels). On the T1 image, the ventricles appear to be dark and the infarct seen in the left lenticular nucleus is dark as well. The T2 image is a lower cut through the center of the infarct. The T2 image shows the CSF within the ventricles to be white. The infarct appears as a white lesion in the caudate nucleus and the left putamen. In the T2 image, internal capsule is dark. Note the obvious distortion of the anterior limb of the left internal capsule, compared to the right. The posterior limb of the left internal capsule is also slightly distorted (compared to the right) adjacent to the infarct in the putamen. This study is read as an infarct in the left basal ganglia, the posterior limb of internal capsule, and the head of the caudate. The structures of this T2 image are labeled if you have difficulty identifying the structures.
The Vest™ Airway Clearance System - Airway Clearance Indications Of Moyamo
Google Directory Health Conditions and Diseases Rare E-Medicine moyamoya disease - http//www.emedicine.com/neuro/topic616.htm moyamoya disease - http//chorus.rad.mcw.edu/doc/01076.html
http://www.abivest.com/conditions/factsheets/moyamoya.asp?gs=patients
Arch Neurol -- Abstract: Moyamoya Disease. Posterior Cerebral Artery Occlusion A
moyamoya disease. Posterior cerebral artery occlusion and Although vascularabnormality in moyamoya disease predominates in the anterior and middle
http://archneur.ama-assn.org/cgi/content/abstract/46/5/550

Extractions: Vol. 46 No. 5, May 1989 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Tashima-Kurita S Fukui M Contact me when this article is cited S. Tashima-Kurita, T. Matsushima, M. Kato, T. Morioka, Y. Kuwabara, K. Hasuo and M. Fukui Department of Neurophysiology, Faculty of Medicine, Kyushu University, Fukuoka, Japan. Although vascular abnormality in moyamoya disease predominates in the anterior and middle cerebral arteries, the posterior cerebral artery (PCA) has been found to be involved in the course of the disease. To explore PCA occlusion by noninvasive means, we studied visual-evoked potentials in the
Arch Neurol -- Abstract: Moyamoya Disease In A Patient With Type I Glycogenosis,
This represents yet another disorder associated with moyamoya disease, which isconsidered to be a secondary phenomenon of vascular occlusion that occurs
http://archneur.ama-assn.org/cgi/content/abstract/38/4/251

Extractions: Vol. 38 No. 4, April 1981 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Sunder TR Contact me when this article is cited T. R. Sunder A 17-year-old boy with type I glycogen storage disease (GSD-I) and a stroke associated with moyamoya disease is described. This is the first report of this association, and only the second reported case of cerebrovascular disease in patients with GSD-I. The relationship of the primary metabolic error and the vascular injury is explored. This represents yet another disorder associated with moyamoya disease, which is considered to be a secondary phenomenon of vascular occlusion that occurs under a specific set of circumstances in a susceptible age group.
Penn State Faculty Research Expertise Database (FRED)
The condition may be idiopathic (classic moyamoya disease) or occur in association Cerebrovascular moyamoya disease, Progressive Intracranial Occlusive
http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D009072

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