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Systemic lupus erythematosus in a man with Noonan syndrome

dc.contributor.authorMartin, Donna M.en_US
dc.contributor.authorGencyuz, Charisse F.en_US
dc.contributor.authorPetty, Elizabeth M.en_US
dc.date.accessioned2006-04-19T13:44:26Z
dc.date.available2006-04-19T13:44:26Z
dc.date.issued2001-07-22en_US
dc.identifier.citationMartin, Donna M.; Gencyuz, Charisse F.; Petty, Elizabeth M. (2001)."Systemic lupus erythematosus in a man with Noonan syndrome." American Journal of Medical Genetics 102(1): 59-62. <http://hdl.handle.net/2027.42/34658>en_US
dc.identifier.issn0148-7299en_US
dc.identifier.issn1096-8628en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34658
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11471173&dopt=citationen_US
dc.description.abstractNoonan syndrome is a multiple congenital anomaly condition characterized by craniofacial anomalies, short stature, cardiac malformations, and normal peripheral blood karyotype analysis. Prior reports of individuals with Noonan syndrome have revealed an association with several autoimmune diseases, including vasculitis and anterior uveitis, but no reports of systemic lupus erythematosus (SLE). Here we present the first case report of a 21-year-old man with a clinical diagnosis of Noonan syndrome and a recent history of mitral valve dysfunction and systemic lupus erythematosus. We discuss his findings in the context of known features of Noonan syndrome and propose that individuals with Noonan syndrome be regularly monitored for associated autoimmune phenomena. © 2001 Wiley-Liss, Inc.en_US
dc.format.extent200800 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherGeneticsen_US
dc.titleSystemic lupus erythematosus in a man with Noonan syndromeen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pediatrics and Communicable Diseases, The University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Internal Medicine, The University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Internal Medicine, The University of Michigan, Ann Arbor, Michigan ; Department of Human Genetics, The University of Michigan, Ann Arbor, Michigan ; Departments of Internal Medicine and Human Genetics, 4301 MSRB III, The University of Michigan, Ann Arbor, MI 48109.en_US
dc.identifier.pmid11471173en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34658/1/1351_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/1096-8628(20010722)102:1<59::AID-AJMG1351>3.0.CO;2-Oen_US
dc.identifier.sourceAmerican Journal of Medical Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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