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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Detalles Bibliográficos
Autores principales: Zama, Daniele, Muratore, Edoardo, Giannetti, Arianna, Neri, Iria, Conti, Francesca, Magini, Pamela, Ferrari, Simona, Pession, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8417938/
https://www.ncbi.nlm.nih.gov/pubmed/34490168
http://dx.doi.org/10.3389/fped.2021.716786

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8417938/
https://www.ncbi.nlm.nih.gov/pubmed/34490168
http://dx.doi.org/10.3389/fped.2021.716786

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