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Article

The clinical course of a child with CINCA/NOMID syndrome improved during and after treatment with thalidomide.

Scandinavian journal of rheumatology - 1 Jan 2000

Kallinich T, Hoffman H M, Roth J, Keitzer R

Abstract excerpt

Chronic, infantile, neurological, cutaneous, and articular (CINCA) syndrome, also known as neonatal-onset multisystem inflammatory disease (NOMID), is a rare autosomal dominant inherited disease. It is characterized by a persistent rash with onset during the neonatal period, neurological and ocular manifestations, and articular involvement with abnormal ossification. Mutations within the CIAS1 gene are found in...

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Identifiers

PMID: 16134734
DOI: 10.1080/03009740410010236

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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.

Related research

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The clinical course of a child with CINCA/NOMID syndrome improved during and after treatment with thalidomide.PMID 16134734Read ↗

Neonatal treatment of CINCA syndrome.Semantic proximity Read ↗

Good response to IL-1beta blockade by anakinra in a 23-year-old CINCA/NOMID patient without mutations in the CIAS1 gene. Cytokine profiles and functional studies.Semantic proximity Read ↗

[Significant effect of IL-1 receptor antagonist treatment in two patients who had CINCA syndrome with constant symptoms for 13 years].Semantic proximity Read ↗

Current status of understanding the pathogenesis and management of patients with NOMID/CINCA.Semantic proximity Read ↗

Chronic Infantile Neurological Cutaneous and Articular (CINCA) syndrome: a review.Semantic proximity Read ↗

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

Detection of a novel mutation in NLRP3/CIAS1 gene in an Indian child with Neonatal-Onset Multisystem Inflammatory Disease (NOMID).Semantic proximity Read ↗

CIAS1 mutation in a patient with overlap between Muckle-Wells and chronic infantile neurological cutaneous and articular syndromes.Semantic proximity Read ↗

Neonatal-onset multisystem inflammatory disease responsive to interleukin-1beta inhibition.Semantic proximity Read ↗

Delayed reactivation of chronic infantile neurologic, cutaneous, articular syndrome (CINCA) in a patient with somatic mosaicism of CIAS1/NLRP3 gene after withdrawal of anti-IL-1 beta therapy.Semantic proximity Read ↗

De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): a new member of the expanding family of pyrin-associated autoinflammatory diseases.Semantic proximity Read ↗

[Syndrome CINCA/NOMID].Semantic proximity Read ↗

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