Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2010-12-14
pubmed:abstractText
A 5-year-old girl with hereditary spherocytosis presented with two episodes of transient ischemic attacks within a month. Cranial magnetic resonance imaging angiography revealed a left internal carotid artery and middle cerebral artery stenosis, with an extensive vascular mesh in the thalamic area indicative of moyamoya disease. Treatment consisted of supporting cerebral perfusion with blood transfusions, and splenectomy to prevent recurrence. Moyamoya disease is a very unusual cerebrovascular disorder in childhood and its association with hereditary spherocytosis is rarely reported.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1873-5150
pubmed:author
pubmed:copyrightInfo
Copyright © 2011 Elsevier Inc. All rights reserved.
pubmed:issnType
Electronic
pubmed:volume
44
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
69-71
pubmed:meshHeading
pubmed-meshheading:21147392-Anemia, pubmed-meshheading:21147392-Blood Transfusion, pubmed-meshheading:21147392-Brain Ischemia, pubmed-meshheading:21147392-Carotid Stenosis, pubmed-meshheading:21147392-Cerebral Angiography, pubmed-meshheading:21147392-Cerebrovascular Circulation, pubmed-meshheading:21147392-Child, Preschool, pubmed-meshheading:21147392-Female, pubmed-meshheading:21147392-Hemoglobins, pubmed-meshheading:21147392-Humans, pubmed-meshheading:21147392-Intelligence Tests, pubmed-meshheading:21147392-Magnetic Resonance Angiography, pubmed-meshheading:21147392-Magnetic Resonance Imaging, pubmed-meshheading:21147392-Middle Cerebral Artery, pubmed-meshheading:21147392-Moyamoya Disease, pubmed-meshheading:21147392-Spherocytosis, Hereditary, pubmed-meshheading:21147392-Splenectomy, pubmed-meshheading:21147392-Stroke, pubmed-meshheading:21147392-Wechsler Scales
pubmed:year
2011
pubmed:articleTitle
Moyamoya disease associated with hereditary spherocytosis.
pubmed:affiliation
Department of Pediatrics, University Hospital Center Reims, Reims, France. pvovan@wanadoo.fr
pubmed:publicationType
Journal Article, Case Reports