Clinical and laboratory features of patients diagnosed with alpha‐gal syndrome—2010–2019

BACKGROUND: Alpha‐gal syndrome (AGS) is an IgE‐mediated allergy to galactose‐alpha‐1,3‐galactose. Clinical presentation ranges from hives to anaphylaxis; episodes typically occur 2–6 h after exposure to alpha‐gal‐containing products. In the United States, lone star tick bites are associated with the...

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Detalles Bibliográficos
Autores principales: Binder, Alison M., Cherry‐Brown, Dena, Biggerstaff, Brad J., Jones, Emma S., Amelio, Claire L., Beard, Charles B., Petersen, Lyle R., Kersh, Gilbert J., Commins, Scott P., Armstrong, Paige A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
ORIGINAL ARTICLES
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092820/
https://www.ncbi.nlm.nih.gov/pubmed/36178236
http://dx.doi.org/10.1111/all.15539

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092820/
https://www.ncbi.nlm.nih.gov/pubmed/36178236
http://dx.doi.org/10.1111/all.15539

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