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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
Publisher
Centro Hospitalar Universitário do Porto