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Article

Familial Eosinophilic Granulomatosis with Polyangiitis in a Sister and Brother.

Internal medicine (Tokyo, Japan) - 1 Apr 2020

Ueki Yuriko, Oshikata Chiyako, Asai Yoshihito, Kaneko Takeshi, Tsurikisawa Naomi

Abstract excerpt

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 2.4 to 14 per million adults. There is little knowledge about the genetic factors that influence this disease. There...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 31813915
DOI: 10.2169/internalmedicine.3744-19
PMCID: PMC7184070

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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