Silva, Joana VanessaFerreira, JoanaSilva, MarianaCosta, Miguel2022-11-302022-11-302021-12Nascer e Crescer - Birth and Growth Medical Journal 2021;30(4):249-251. doi:10.25753/BirthGrowthMJ.v30.i4.200602183-9417http://hdl.handle.net/10400.16/2757Bisalbuminemia 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.engblood protein disorderelectrophoresisserum albuminBiochemical clinical caseCaso clínico bioquímicojournal articlehttps://doi.org/10.25753/BirthGrowthMJ.v30.i4.20060