Wilson Disease in Children

Clin Liver Dis. 2022 Aug;26(3):473-488. doi: 10.1016/j.cld.2022.03.008. Epub 2022 Jun 25.

Abstract

The silver anniversary of the discovery of the Wilson disease gene ATP7B was a couple of years ago, and we continue to make progress both in our understanding of copper transportation using animal models as well as earlier diagnosis by availing of genetic testing. Wilson disease is multisystemic and the hepatic manifestations are seen more frequently in childhood, whereas neurologic manifestations are more common in adults; presentation may range from subtle changes to end-stage liver disease with or without encephalopathy as well as neuropsychiatric manifestations. Treatment remains with zinc and chelating agents such as D-penicillamine and trientine but newer agents and gene therapy are in clinical trials. Liver transplantation becomes necessary when medical therapy is not enough. Molecular diagnosis and genetic counseling is important.

Keywords: ATP7B; Acute liver failure; Chelating agents; Cirrhosis; Copper metabolism; Wilson disease.

Publication types

  • Review

MeSH terms

  • Chelating Agents / therapeutic use
  • Copper / therapeutic use
  • Hepatolenticular Degeneration* / diagnosis
  • Hepatolenticular Degeneration* / genetics
  • Hepatolenticular Degeneration* / therapy
  • Humans
  • Penicillamine / therapeutic use
  • Trientine / therapeutic use

Substances

  • Chelating Agents
  • Copper
  • Penicillamine
  • Trientine