Case Report: Hereditary Alpha Tryptasemia in Children: A Pediatric Case Series and a Brief Overview of Literature

Case Report: Hereditary Alpha Tryptasemia in Children: A Pediatric Case Series and a Brief Overview of Literature

Hereditary alpha tryptasemia (HαT) is a recently described autosomal dominant genetic trait caused by an increased copy number of the TPSAB1 gene. It commonly leads to elevated basal serum tryptase levels, and it is associated with heterogeneous clinical manifestations. Some individuals report few t...

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Bibliographic Details
Main Authors: Daniele Zama, Edoardo Muratore, Arianna Giannetti, Iria Neri, Francesca Conti, Pamela Magini, Simona Ferrari, Andrea Pession
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-08-01
Series:Frontiers in Pediatrics
Subjects:
hereditary alpha tryptasemia
mastocytosis
mast cell activation syndrome
pediatric allergology
genetic disorder
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2021.716786/full

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