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dc.contributor.authorArdalan, M
dc.contributor.authorVahedi, A
dc.date.accessioned2018-08-26T06:05:59Z
dc.date.available2018-08-26T06:05:59Z
dc.date.issued2013
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/41908
dc.description.abstractAntiphospholipid syndrome (APS) is a systemic disorder characterizes by recurrent arterial and venous thrombosis and/or pregnancy miscarriages and positive test for antiphospholipid antibodies.Here we report a 31 year-old female whose main complain was symmetrical motor polyneuropathy and hand muscular weakness over a long period of time. Her clinical picture became more complex by Mitral valve regurgitation and renal dysfunction. Finally with the diagnosis of APS glucocorticoid therapy was started and her renal dysfunction improved profoundly, however her cardiac valvular involvement and peripheral neuropathy remained.APS is a disease with wide clinical presentations and it continues to confound the clinicians.
dc.language.isoEnglish
dc.relation.ispartofJournal of nephropathology
dc.titleAntiphospholipid syndrome: A disease of protean face.
dc.typearticle
dc.citation.volume2
dc.citation.issue1
dc.citation.spage81
dc.citation.epage4
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.5812/nephropathol.9001


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