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Article

Hyperimmunoglobulinemia D syndrome in an Arab child.

Clinical rheumatology - 1 Feb 2005

Hammoudeh Mohammed

Abstract excerpt

Hyperimmunoglobulinemia D syndrome (HIDS) is newly recognized and resembles familial Mediterranean fever (FMF). It is inherited as an autosomal recessive trait. Mutation of the gene coding for mevalonate kinase is responsible for the disease. The gene is located at chromosome 12q24. The patients initially described were of Dutch ancestry. Other cases from Turkey and Armenia were reported. The case we present is...

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Identifiers

PMID: 15674660
DOI: 10.1007/s10067-004-0953-0

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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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