Advancing diagnosis and research for rare genetic diseases in Indigenous peoples

Nat Genet. 2024 Feb;56(2):189-193. doi: 10.1038/s41588-023-01642-1.

Abstract

Achieving a diagnosis for Indigenous people living with a rare, often genetic, disease is crucial for equitable healthcare. The International Rare Disease Research Consortium convened a global Task Force to bridge the gap in diagnosing Indigenous rare diseases, and identify solutions to tackle the health inequity faced by Indigenous people.

MeSH terms

  • Humans
  • Indigenous Peoples*
  • Rare Diseases* / diagnosis
  • Rare Diseases* / genetics