Your browser doesn't support javascript.
loading
[Moyamoya disease in children] / Moyamoya hos barn.
Fric, Radek; Sorteberg, Angelika; Wallace, Sean; Alonso, Andres Server; Due-Tønnessen, Bernt Johan; Wiedmann, Markus.
Affiliation
  • Fric R; Nevrokirurgisk avdeling, Nevroklinikken, Oslo universitetssykehus, Rikshospitalet.
  • Sorteberg A; Nevrokirurgisk avdeling, Nevroklinikken, Oslo universitetssykehus, Rikshospitalet, og, Institutt for klinisk medisin, Universitetet i Oslo.
  • Wallace S; Barneavdeling for nevrofag, Oslo universitetssykehus, Rikshospitalet.
  • Alonso AS; Avdeling for radiologi og nukleær medisin, Oslo universitetssykehus, Rikshospitalet.
  • Due-Tønnessen BJ; Nevrokirurgisk avdeling, Nevroklinikken, Oslo universitetssykehus, Rikshospitalet.
  • Wiedmann M; Nevrokirurgisk avdeling, Nevroklinikken, Oslo universitetssykehus, Rikshospitalet.
Tidsskr Nor Laegeforen ; 142(13)2022 09 27.
Article in Nor | MEDLINE | ID: mdl-36164799
ABSTRACT
Moyamoya is a rare condition that affects the blood vessels of the brain in children and young adults. It can cause both ischaemic stroke and cerebral haemorrhage. Although established diagnostic criteria and examinations exist, limited knowledge of the condition often leads to a mistaken or delayed diagnosis. Treatment consists of antiplatelet drugs and surgical revascularisation. Prognosis after successful surgery is good, but the disease requires a dedicated medical team.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Ischemia / Stroke / Moyamoya Disease Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Adult / Child / Humans Language: Nor Journal: Tidsskr Nor Laegeforen Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Ischemia / Stroke / Moyamoya Disease Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Adult / Child / Humans Language: Nor Journal: Tidsskr Nor Laegeforen Year: 2022 Document type: Article