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Bisalbuminemia: A Rare Variant of Albumin

dc.contributor.authorGarcez, C
dc.contributor.authorCarvalho, S
dc.date.accessioned2017-06-02T15:32:08Z
dc.date.available2017-06-02T15:32:08Z
dc.date.issued2017-04-28
dc.description.abstractINTRODUCTION: Bisalbuminemia is a qualitative disorder of albumin and it is defined by the coexistence in the same individual of two types of serum albumin with different electrophoretic mobility. There are two forms: hereditary and permanent, or acquired and transient. CASE REPORT: Girl, 17-years-old, referenced to the hospital consult after incidental finding of bisalbuminemia detected in plasma protein electrophoresis performed within the investigation of diminished muscular tone in the lower limbs. Physical examination was normal. Secondary causes of bisalbuminemia were excluded. Later, it was confirmed the same disorder in plasma protein electrophoresis performed to her 14-years-old brother and mother. DISCUSSION: We describe a rare case of hereditary bisalbuminemia in a portuguese family. In general, this condition shows no pathological significance, however it is of interest to the clinicians the knowledge of this analytic change for better orientation of their patients.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationActa Med Port. 2017 Apr 28;30(4):330-333pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.23/1182
dc.language.isoporpt_PT
dc.peerreviewedyespt_PT
dc.subjectAlbuminapt_PT
dc.subjectAlterações Proteínas Sanguíneaspt_PT
dc.titleBisalbuminemia: A Rare Variant of Albuminpt_PT
dc.title.alternativeBisalbuminémia: Uma Variante Rara da Albuminapt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue4pt_PT
oaire.citation.startPage330-333pt_PT
oaire.citation.volume30pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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