Publication Date

11-2021

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Abstract

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.

Disciplines

Allergy and Immunology | Pediatrics

Notes

Presented at the American College of Allergy, Asthma, and Immunology, New Orleans, November 4-8th, 2021.

A case of an elevated tryptase

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