Molecular Genetics and Modifier Genes in Pseudoxanthoma Elasticum, a Heritable Multisystem Ectopic Mineralization Disorder

J Invest Dermatol. 2021 May;141(5):1148-1156. doi: 10.1016/j.jid.2020.10.013. Epub 2020 Dec 17.

Abstract

In the past two decades, there has been great progress in identifying the molecular basis and pathomechanistic details in pseudoxanthoma elasticum (PXE), a heritable multisystem ectopic mineralization disorder. Although the identification of pathogenic variants in ABCC6 has been critical for understanding the disease process, genetic modifiers have been disclosed that explain the phenotypic heterogeneity of PXE. Adding to the genetic complexity of PXE are PXE-like phenotypes caused by pathogenic variants in other ectopic mineralization-associated genes. This review summarizes the current knowledge of the genetics and candidate modifier genes in PXE, a multifactorial disease at the genome-environment interface.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Diphosphates / metabolism
  • Genetic Association Studies
  • Humans
  • Mice
  • Multidrug Resistance-Associated Proteins / genetics*
  • Oxidative Stress
  • Phosphoric Diester Hydrolases / genetics
  • Pseudoxanthoma Elasticum / genetics*
  • Pyrophosphatases / genetics
  • Vascular Calcification

Substances

  • ABCC6 protein, human
  • Diphosphates
  • Multidrug Resistance-Associated Proteins
  • diphosphoric acid
  • Phosphoric Diester Hydrolases
  • ectonucleotide pyrophosphatase phosphodiesterase 1
  • Pyrophosphatases