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Article

Hyper-IgD syndrome or mevalonate kinase deficiency.

Current opinion in rheumatology - 1 Sept 2011

Stoffels Monique, Simon Anna

Abstract excerpt

PURPOSE OF REVIEW: The hyper-IgD and periodic fever syndrome (HIDS) is one of the classical monogenetic hereditary autoinflammatory disorders, and together with the more severe mevalonic aciduria it is also known as 'mevalonate kinase deficiency' (MKD). In this study, we will give an overview of the primary research on mevalonate kinase deficiency published in the past 2 years. RECENT FINDINGS: Besides an...

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Identifiers

PMID: 21760510
DOI: 10.1097/BOR.0b013e328349c3b1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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