Hyper-IgD syndrome/mevalonate kinase deficiency: what is new?

Abstract

Mevalonate kinase deficiency or hyper-IgD syndrome is a hereditary autoinflammatory syndrome caused by mutations in the mevalonate kinase gene. In this review, we will discuss new findings in this disorder that have been published in the last 2 years. This includes new insights into pathophysiology, treatment, and the clinical phenotype linked to the… (More)
DOI: 10.1007/s00281-015-0492-6

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