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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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| Publicado en: | Intern Med |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
The Japanese Society of Internal Medicine
2019
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| Assuntos: | |
| Acceso en liña: | 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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