Repository logo
 
Loading...
Thumbnail Image
Publication

Biochemical clinical case

Use this identifier to reference this record.
Name:Description:Size:Format: 
20060-Article Text-105253-1-10-20211227.pdf277.15 KBAdobe PDF Download

Advisor(s)

Abstract(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.

Description

Keywords

blood protein disorder electrophoresis serum albumin

Citation

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

Research Projects

Organizational Units

Journal Issue

Publisher

Centro Hospitalar Universitário do Porto

Altmetrics