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

• Κύριοι συγγραφείς: Daniele Zama (Συγγραφέας), Edoardo Muratore (Συγγραφέας), Arianna Giannetti (Συγγραφέας), Iria Neri (Συγγραφέας), Francesca Conti (Συγγραφέας), Pamela Magini (Συγγραφέας), Simona Ferrari (Συγγραφέας), Andrea Pession (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: Frontiers Media S.A., 2021-08-01T00:00:00Z.
• Θέματα: article
• Διαθέσιμο Online: 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...