Acrodermatitis enteropathica-like syndrome secondary to isoleucine deficiency during treatment of maple syrup urine disease

Am J Dis Child. 1993 Sep;147(9):954-6. doi: 10.1001/archpedi.1993.02160330044015.

Abstract

We describe a patient with maple syrup urine disease in whom an acrodermatitis enteropathica-like syndrome developed while he was receiving a branched-chain amino acid-free formula. Iatrogenically induced isoleucine deficiency developed and resulted in a decreased protein accretion and persistent increase in the plasma concentrations of leucine. A rapid clinical response to isoleucine supplementation was noted. This observation underscores the risks of using amino acid-free formulas without adequate supplementation of deficient amino acids.

Publication types

  • Case Reports

MeSH terms

  • Acrodermatitis / etiology*
  • Humans
  • Iatrogenic Disease
  • Infant Food
  • Infant, Newborn
  • Isoleucine / deficiency*
  • Male
  • Maple Syrup Urine Disease / complications*
  • Maple Syrup Urine Disease / diet therapy
  • Syndrome

Substances

  • Isoleucine