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

• Main Authors: Daniele Zama (Author), Edoardo Muratore (Author), Arianna Giannetti (Author), Iria Neri (Author), Francesca Conti (Author), Pamela Magini (Author), Simona Ferrari (Author), Andrea Pession (Author)
• Format: Book
• Published: Frontiers Media S.A., 2021-08-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...