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Biochemical clinical case

dc.contributor.authorSilva, Joana Vanessa
dc.contributor.authorFerreira, Joana
dc.contributor.authorSilva, Mariana
dc.contributor.authorCosta, Miguel
dc.date.accessioned2022-11-30T11:03:55Z
dc.date.available2022-11-30T11:03:55Z
dc.date.issued2021-12
dc.description.abstractBisalbuminemia is a qualitative albumin variation defined by coexistence of two types of serum albumin with different electrophoretic mobilities in the same individual. It can be of two different types: hereditary (or permanent) and acquired (or transient). Herein is described a rare case of hereditary bisalbuminemia in a healthy infant, incidentally found during elevated aminotransferase study. Despite not having pathological significance, acknowledgement of this analytical alteration is key for adequate management of these patients.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationNascer e Crescer - Birth and Growth Medical Journal 2021;30(4):249-251. doi:10.25753/BirthGrowthMJ.v30.i4.20060pt_PT
dc.identifier.doihttps://doi.org/10.25753/BirthGrowthMJ.v30.i4.20060pt_PT
dc.identifier.issn2183-9417
dc.identifier.urihttp://hdl.handle.net/10400.16/2757
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherCentro Hospitalar Universitário do Portopt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt_PT
dc.subjectblood protein disorderpt_PT
dc.subjectelectrophoresispt_PT
dc.subjectserum albuminpt_PT
dc.titleBiochemical clinical casept_PT
dc.title.alternativeCaso clínico bioquímicopt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlacePortopt_PT
oaire.citation.endPage251pt_PT
oaire.citation.issue4pt_PT
oaire.citation.startPage249pt_PT
oaire.citation.titleNascer e Crescer - Birth and Growth Medical Journalpt_PT
oaire.citation.volume30pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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