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Hereditary Alpha Tryptasemia (HαT) is an autosomal dominant disorder characterized by an elevated baseline tryptase that occurs up to 3% of the population and clinically resembles mast cell activation syndrome.
Allergy and Immunology | Pediatrics
Parashar, Sonya and Raje, Nikita, "A case of an elevated tryptase" (2021). Posters. 242.