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Article

Current status of understanding the pathogenesis and management of patients with NOMID/CINCA.

Current rheumatology reports - 1 Apr 2011

Goldbach-Mansky Raphaela

Abstract excerpt

Neonatal-onset multisystem inflammatory disease (NOMID)/chronic infantile neurologic, cutaneous, and arthritis (CINCA) syndrome is the most severe clinical phenotype in the spectrum of cryopyrin- (NLRP3/NALP3) associated periodic syndromes (CAPS). The study of patients with NOMID/CINCA has been instrumental in characterizing the extent of organ-specific inflammatory manifestations and damage that can occur with...

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Share to Antirheumatic Agents
Share to Cryopyrin-Associated Periodic Syndromes
Share to Drug Evaluation, Preclinical

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn, Diseases

Share to Inflammasomes

Share to Interleukin 1 Receptor Antagonist Protein

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Share to NLR Family, Pyrin Domain-Containing 3 Protein

Source

Open in PubMed Open full text

Identifiers

PMID: 21538043
DOI: 10.1007/s11926-011-0165-y
PMCID: PMC3195512

Genes

NLRP3
CAPS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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