Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathways

Mol Genet Metab. 2000 Sep-Oct;71(1-2):10-8. doi: 10.1006/mgme.2000.3066.

Abstract

Inborn errors of metabolism show considerable variation in the severity of symptoms. This is often ascribed to the differential effects of specific mutations on gene/enzyme function; however, such genotype/phenotype correlations are usually imprecise. In addition, in some patients with clinical and biochemical findings consistent with a defect in a particular metabolic pathway, it is ultimately impossible to arrive at a precise enzymatic diagnosis. In this situation, we have increasingly been identifying concurrent partial defects in more than one pathway, or at multiple steps in one pathway. In this study, we present the clinical, biochemical, and molecular findings from several patients showing multiple partial defects in energy metabolism. These patients show clinical symptoms consistent with a defect in the affected pathways even though they do not have a complete deficiency in any one enzyme. We hypothesize that such patients are exhibiting clinically significant reductions in energy metabolism related to the compound effects of these partial defects, a phenomenon we term "synergistic heterozygosity." Based on the frequencies of known disorders of energy metabolism, we propose that this may represent a previously unrecognized, relatively common mechanism of disease of potentially great clinical relevance.

Publication types

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

MeSH terms

  • AMP Deaminase / deficiency
  • AMP Deaminase / genetics
  • Acyl-CoA Dehydrogenase, Long-Chain
  • Adolescent
  • Adult
  • Carnitine O-Palmitoyltransferase / deficiency
  • Carnitine O-Palmitoyltransferase / genetics
  • Child
  • Energy Metabolism
  • Fatty Acid Desaturases / deficiency
  • Fatty Acid Desaturases / genetics
  • Female
  • Glycogen Storage Disease Type V / enzymology
  • Glycogen Storage Disease Type V / genetics
  • Heterozygote
  • Humans
  • Infant
  • Male
  • Metabolism, Inborn Errors / genetics*
  • Metabolism, Inborn Errors / metabolism*
  • Models, Biological
  • Mutation
  • Phenotype

Substances

  • Fatty Acid Desaturases
  • Acyl-CoA Dehydrogenase, Long-Chain
  • Carnitine O-Palmitoyltransferase
  • AMP Deaminase