Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuria

Neurology. 1998 Jan;50(1):296-8. doi: 10.1212/wnl.50.1.296.

Abstract

A 14-year-old boy with exercise-related myalgia and cramps had several episodes of myoglobinuria since early childhood. An episode at 2 years of age caused acute renal failure. Histochemical and biochemical analysis of muscle showed a combined defect of phosphofructokinase (PFK) and adenosine monophosphate (AMP) deaminase. DNA analysis showed that the patient was homozygous for a G-to-C substitution at codon 39 of the PFK gene (previously described in an Italian patient) and for the common mutation found in AMP deaminase deficiency.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP Deaminase / genetics*
  • Adolescent
  • Biopsy
  • DNA Mutational Analysis
  • Homozygote
  • Humans
  • Male
  • Muscle, Skeletal / enzymology
  • Muscle, Skeletal / pathology
  • Mutation
  • Myoglobinuria / enzymology*
  • Myoglobinuria / genetics*
  • Myoglobinuria / pathology
  • Phosphofructokinase-1 / genetics*
  • Polymerase Chain Reaction

Substances

  • Phosphofructokinase-1
  • AMP Deaminase