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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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Bibliografski detalji
Izdano u:Intern Med
Glavni autori: Ueki, Yuriko, Oshikata, Chiyako, Asai, Yoshihito, Kaneko, Takeshi, Tsurikisawa, Naomi
Format: Artigo
Jezik:Inglês
Izdano: The Japanese Society of Internal Medicine 2019
Teme:
Online pristup: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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