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Biochemical clinical case

2021-12Artigo científico Acesso aberto
http://hdl.handle.net/10400.16/2757
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Autores

Silva, Joana Vanessa
Ferreira, Joana
Silva, Mariana
Costa, Miguel

Orientador(es)

Resumo(s)

Bisalbuminemia 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.

Descrição

Palavras-chave

blood protein disorder electrophoresis serum albumin

URI

http://hdl.handle.net/10400.16/2757

Contexto Educativo

Citação

Nascer e Crescer - Birth and Growth Medical Journal 2021;30(4):249-251. doi:10.25753/BirthGrowthMJ.v30.i4.20060

Projetos de investigação

Unidades organizacionais

Fascículo

Editora

Centro Hospitalar Universitário do Porto

DOI

https://doi.org/10.25753/BirthGrowthMJ.v30.i4.20060

Coleções

RN&C: Ano de 2021

Licença CC

cclicense-by-nc

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