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Hereditary alpha-tryptasemia

4 Aug 2022

Abstract excerpt

PURPOSE OF REVIEW: To discuss our evolving knowledge about the genetic variations in human tryptase and recent advances in associated clinical phenotypes. RECENT FINDINGS: Hereditary alpha-tryptasemia (HAT) is an autosomal dominant genetic trait and a common cause of elevated basal serum tryptase (BST) in Western populations. It is a risk factor for severe anaphylaxis and an established modifier of mast cell...

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PMID: 35942852
DOI: 10.1097/aci.0000000000000849

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