Literature DB >> 10437648

Bisalbuminuria in an adult with bisalbuminemia and nephrotic syndrome.

M P Hoang1, L B Baskin, F H Wians.   

Abstract

Bisalbuminemia (or alloalbuminemia) is a relatively rare hereditary or acquired condition characterized by the presence of two distinct albumin bands, or, less commonly, a single widened albumin band, after agarose gel electrophoresis of serum. Bisalbumins are caused by point- or chain-mutations that occur with a population frequency of 1:10,000 to 1:1000. Although no adverse clinical effects have been attributed to bisalbumins, some albumin variants have altered affinity for steroid hormones, thyroxine, or drugs. We report a case of bisalbuminuria in a 25-year-old man with bisalbuminemia and nephrotic syndrome.

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Year:  1999        PMID: 10437648     DOI: 10.1016/s0009-8981(99)00054-6

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  2 in total

1.  Detection of hereditary bisalbuminemia in a Greek family by capillary zone electrophoresis.

Authors:  C Angouridaki; V Papageorgiou; V Tsavdaridou; M Giannousis; S Alexiou-Daniel
Journal:  Hippokratia       Date:  2008-04       Impact factor: 0.471

2.  Bisalbuminemia in a Hypothyroid Patient with Diabetes: A Case Report.

Authors:  Jeevan K Shetty; Ravindra Maradi; Krishnananda Prabhu; Gopalkrishna Bhat
Journal:  J Clin Diagn Res       Date:  2015-09-01
  2 in total

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