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Article

Blau syndrome with pulmonary nodule in a child.

The Australasian journal of dermatology - 1 May 2021

Su Jinping, Liu Donghua

Abstract excerpt

Blau syndrome (BS) is a rare monogenic disease caused by mutation of NOD2/CARD15 gene. A case of Blau syndrome in a 4-year-old Chinese boy c.1001G > A(p.R334Q) mutation in the NOD2 genes reported. Imaging revealed a nodule at the tip of the right lung.

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Identifiers

PMID: 33742458
DOI: 10.1111/ajd.13551

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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