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Article

Two German CINCA (NOMID) patients with different clinical severity and response to anti-inflammatory treatment.

European journal of haematology - 1 Sept 2003

Rösen-Wolff Angela, Quietzsch Jürgen, Schröder Heinz, Lehmann Romy, Gahr Manfred, Roesler Joachim

Abstract excerpt

Chronic infantile neurologic, cutaneous, articular (CINCA) syndrome is characterized by fever, chronic meningitis, uveitis, sensorineural hearing loss, urticarial skin rash, and a deforming arthritis. In the CIAS1 gene of many but not all CINCA patients, disease-associated mutations have been found recently. We here describe two such patients from Germany. One of them, a 3-yr-old boy, has a 1709A-->G, Y570C,...

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Identifiers

PMID: 12930324
DOI: 10.1034/j.1600-0609.2003.00109.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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