Diagnosis of rare bleeding disorders

Haemophilia. 2022 May:28 Suppl 4:119-124. doi: 10.1111/hae.14561.

Abstract

Rare bleeding disorders result in significant morbidity but are globally underdiagnosed. Advances in genomic testing and specialist laboratory assays have greatly increased the diagnostic armamentarium. This has resulted in the discovery of new genetic causes for rare diseases and a better understanding of the underlying molecular pathology.

Keywords: blood coagulation disorders; blood platelet disorders; hemorrhagic disorders; whole exome sequencing; whole genome sequencing.

MeSH terms

  • Blood Coagulation Disorders* / diagnosis
  • Blood Platelet Disorders* / genetics
  • Hemorrhage / diagnosis
  • Hemorrhage / etiology
  • Hemorrhagic Disorders* / diagnosis
  • Hemorrhagic Disorders* / genetics
  • Humans
  • Rare Diseases / diagnosis
  • Rare Diseases / genetics