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Article

Muckle-Wells syndrome in an Indian family associated with NLRP3 mutation.

Journal of postgraduate medicine - 1 Jan 2000

Abdulla M C, Alungal J, Hawkins P N, Mohammed S

Abstract excerpt

Muckle-Wells syndrome (MWS) is a rare autosomal dominant disease that belongs to a group of hereditary periodic fever syndromes. It is part of the wider spectrum of the cryopyrin-associated periodic syndrome (CAPS) which has only rarely been described in non-Caucasian individuals. It is characterized by recurrent self-limiting episodes of fever, urticaria, arthralgia, myalgia and conjunctivitis from childhood....

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Open in PubMed Open full text

Identifiers

PMID: 25766347
DOI: 10.4103/0022-3859.153107
PMCID: PMC4943435

Genes

NLRP3
CAPS

Provenance

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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A three-generation Muckle-Wells syndrome family: Detailed family history, physical examination, and inter-departmental collaboration.Semantic proximity Read ↗

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