Early- Onset Stroke and Vasculopathy Associated with Mutations in ADA2

dc.contributor.authorQ. Zhou
dc.contributor.authorD. Yang
dc.contributor.authorA.K. Ombrello
dc.contributor.authorAndrey V. Zavialov
dc.contributor.authorC. Toro
dc.contributor.authorAnton V. Zavialov
dc.contributor.authorD.L. Stone
dc.contributor.authorJ.J. Chae
dc.contributor.authorS.D. Rosenzweig
dc.contributor.authorK. Bishop
dc.contributor.authorK.S. Barron
dc.contributor.authorH.S. Kuehn
dc.contributor.authorP. Hoffmann
dc.contributor.authorA. Negro
dc.contributor.authorW.L. Tsai
dc.contributor.authorE.W. Cowen
dc.contributor.authorW. Pei
dc.contributor.authorJ.D. Milner
dc.contributor.authorC. Silvin
dc.contributor.authorT. Heller
dc.contributor.authorD.T. Chin
dc.contributor.authorN.J. Patronas
dc.contributor.authorJ.S. Barber
dc.contributor.authorC.-C.R. Lee
dc.contributor.authorG.M. Wood
dc.contributor.authorA. Ling
dc.contributor.authorS.J. Kelly
dc.contributor.authorD.E. Kleiner
dc.contributor.authorJ.C. Mullikin
dc.contributor.authorN.J. Ganson
dc.contributor.authorH.H. Kong
dc.contributor.authorS. Hambleton
dc.contributor.authorF. Candotti
dc.contributor.authorM.M. Quezado
dc.contributor.authorK.R. Calvo
dc.contributor.authorH. Alao
dc.contributor.authorB.K. Barham
dc.contributor.authorA. Jones
dc.contributor.authorJ.F. Meschia
dc.contributor.authorB.B. Worrall
dc.contributor.authorS.E. Kasner
dc.contributor.authorS.S. Rich
dc.contributor.authorR. Goldbach-Mansky
dc.contributor.authorM. Abinun
dc.contributor.authorE. Chalom
dc.contributor.authorA.C. Gotte
dc.contributor.authorM. Punaro
dc.contributor.authorV. Pascual
dc.contributor.authorJ.W. Verbsky
dc.contributor.authorT.R. Torgerson
dc.contributor.authorN.G. Singer
dc.contributor.authorT.R. Gershon
dc.contributor.authorS. Ozen
dc.contributor.authorO. Karadag
dc.contributor.authorT.A. Fleisher
dc.contributor.authorE.F. Remmers
dc.contributor.authorS.M. Burgess
dc.contributor.authorS.L. Moir
dc.contributor.authorM. Gadina
dc.contributor.authorR. Sood
dc.contributor.authorM.S. Hershfield
dc.contributor.authorM. Boehm
dc.contributor.authorD.L. Kastner
dc.contributor.authorand I. Aksentijevich
dc.contributor.organizationfi=JBL-laboratorio|en=Joint Biotechnology Laboratory (JBL)|
dc.contributor.organization-code1.2.246.10.2458963.20.53708885453
dc.converis.publication-id3661938
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/3661938
dc.date.accessioned2022-10-28T13:57:50Z
dc.date.available2022-10-28T13:57:50Z
dc.description.abstract<p> Adenosine deaminase 2 (ADA2) is an enzyme involved in purine metabolism and a growth factor that influences the development of endothelial cells and leukocytes. This study shows that defects in ADA2 cause recurrent fevers, vascular pathologic features, and mild immunodeficiency. Patients with autoinflammatory disease sometimes present with clinical findings that encompass multiple organ systems.(1) Three unrelated children presented to the National Institutes of Health (NIH) Clinical Center with intermittent fevers, recurrent lacunar strokes, elevated levels of acute-phase reactants, livedoid rash, hepatosplenomegaly, and hypogammaglobulinemia. Collectively, these findings do not easily fit with any of the known inherited autoinflammatory diseases. Hereditary or acquired vascular disorders can have protean manifestations yet be caused by mutations in a single gene. Diseases such as the Aicardi-Goutieres syndrome,(2),(3) polypoidal choroidal vasculopathy,(4) sickle cell anemia,(5) livedoid vasculopathy,(6) and the small-vessel vasculitides(7),(8) are examples of systemic ...</p>
dc.format.pagerange911
dc.format.pagerange920
dc.identifier.jour-issn0028-4793
dc.identifier.olddbid185467
dc.identifier.oldhandle10024/168561
dc.identifier.urihttps://www.utupub.fi/handle/11111/42285
dc.identifier.urnURN:NBN:fi-fe2021042715266
dc.okm.affiliatedauthorZavialov, Anton
dc.okm.discipline1182 Biochemistry, cell and molecular biologyen_GB
dc.okm.discipline1182 Biokemia, solu- ja molekyylibiologiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherMASSACHUSETTS MEDICAL SOC
dc.relation.doi10.1056/NEJMoa1307361
dc.relation.ispartofjournalNew England Journal of Medicine
dc.relation.issue10
dc.relation.volume370
dc.source.identifierhttps://www.utupub.fi/handle/10024/168561
dc.titleEarly- Onset Stroke and Vasculopathy Associated with Mutations in ADA2
dc.year.issued2014

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From The New England Journal of Medicine, Zhou et al., Early- Onset Stroke and Vasculopathy Associated with Mutations in ADA2, 370, 911-920. Copyright © 2014 Massachusetts Medical Society. Reprinted with permission