A case of an elevated tryptase

Authors

Sonya Parashar, Children's Mercy HopitalFollow
Nikita Raje, Children's Mercy HospitalFollow

Publication Date

11-2021

Files

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.

Recommended Citation

Parashar, Sonya and Raje, Nikita, "A case of an elevated tryptase" (2021). Posters. 242.
https://scholarlyexchange.childrensmercy.org/posters/242