Systemic lupus erythematosus in a man with Noonan syndrome
dc.contributor.author | Martin, Donna M. | en_US |
dc.contributor.author | Gencyuz, Charisse F. | en_US |
dc.contributor.author | Petty, Elizabeth M. | en_US |
dc.date.accessioned | 2006-04-19T13:44:26Z | |
dc.date.available | 2006-04-19T13:44:26Z | |
dc.date.issued | 2001-07-22 | en_US |
dc.identifier.citation | Martin, 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.issn | 0148-7299 | en_US |
dc.identifier.issn | 1096-8628 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/34658 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11471173&dopt=citation | en_US |
dc.description.abstract | Noonan 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.extent | 200800 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | John Wiley & Sons, Inc. | en_US |
dc.subject.other | Life and Medical Sciences | en_US |
dc.subject.other | Genetics | en_US |
dc.title | Systemic lupus erythematosus in a man with Noonan syndrome | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Genetics | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Pediatrics and Communicable Diseases, The University of Michigan, Ann Arbor, Michigan | en_US |
dc.contributor.affiliationum | Department of Internal Medicine, The University of Michigan, Ann Arbor, Michigan | en_US |
dc.contributor.affiliationum | Department 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.pmid | 11471173 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/34658/1/1351_ftp.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1002/1096-8628(20010722)102:1<59::AID-AJMG1351>3.0.CO;2-O | en_US |
dc.identifier.source | American Journal of Medical Genetics | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
Files in this item
Remediation of Harmful Language
The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.
Accessibility
If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.