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Familial Eosinophilic Granulomatosis with Polyangiitis in a Sister and Brother

Eosinophilic granulomatosis with polyangiitis (EGPA) is a vasculitis characterized by an abnormally high number of eosinophils in the peripheral blood and tissues. EGPA is an extremely rare disorder, with an incidence of 0.5 to 3.7 new cases per million people per year and an overall prevalence of 2...

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Detalhes bibliográficos
Publicado no:Intern Med
Main Authors: Ueki, Yuriko, Oshikata, Chiyako, Asai, Yoshihito, Kaneko, Takeshi, Tsurikisawa, Naomi
Formato: Artigo
Idioma:Inglês
Publicado em: The Japanese Society of Internal Medicine 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7184070/
https://ncbi.nlm.nih.gov/pubmed/31813915
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2169/internalmedicine.3744-19
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