Revisiting protein-losing enteropathy: a rare case of chorea

Authors

  • PM Bester University of the Free State
  • WM Simmonds University of the Free State
  • E Osayande University of the Free State

DOI:

https://doi.org/10.36303/SAJGH.2965

Keywords:

protein-losing enteropathy, chorea, vitamin D, malabsorption, technetium 99m-methylene diphosphonate

Abstract

Protein-losing enteropathy is an umbrella term for a diverse group of disorders causing uncompensated plasma protein loss into the gastrointestinal tract in the absence of kidney or liver disease. In a healthy individual, protein loss through the gastrointestinal tract is about 10% of the normal turnover.1 Most plasma proteins in the gastrointestinal tract are broken down into amino acids and  reabsorbed. The liver can compensate for excessive protein loss by increasing its production by up to 2.7 times.2 As soon as protein loss exceeds liver production, signs of protein-losing enteropathy develop. The molecular weight does not influence which proteins are lost; however, proteins with longer half-lives are most affected, whereas those with a rapid turnover are less affected.3 Depending on the cause, patients may also experience malabsorption of other compounds (e.g. fat and fat-soluble vitamins).

Author Biographies

PM Bester, University of the Free State

Department of Internal Medicine, Faculty of Health Sciences, University of the Free State, South Africa

WM Simmonds, University of the Free State

Department of Internal Medicine, Faculty of Health Sciences, University of the Free State, South Africa

E Osayande, University of the Free State

Department of Nuclear Medicine, Faculty of Health Sciences, University of the Free State, South Africa

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Published

2025-08-07

Issue

Section

Case Report