Hyper-IgD syndrome/mevalonate kinase deficiency: what is new?
Hyper-IgD syndrome/mevalonate kinase deficiency: what is new?
About this item
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Author / Creator
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title
Language
English
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Publication information
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
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More information
Scope and Contents
Contents
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 t...
Alternative Titles
Full title
Hyper-IgD syndrome/mevalonate kinase deficiency: what is new?
Authors, Artists and Contributors
Author / Creator
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4491100
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4491100
Other Identifiers
ISSN
1863-2297
E-ISSN
1863-2300
DOI
10.1007/s00281-015-0492-6
