Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[MVK gene abnormality and new approach to treatment of hyper IgD syndrome and periodic fever syndrome].

Nihon Rinsho Men'eki Gakkai kaishi = Japanese journal of clinical immunology - 1 Apr 2007

Naruto Takuya

Abstract excerpt

Hyper IgD and periodic fever syndrome (HIDS; OMIM 260920) is one of the hereditary autoinflammatory syndromes characterized by recurrent episodes of fever and inflammation.. HIDS is an autosomal recessive disorder characterized by recurrent fever attacks in early childhood. HIDS caused by mevalonate kinase (MK) mutations, also that is the gene of mevalonic aciduria (OMIM 251170). During febrile episodes, urinary...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Familial Mediterranean Fever
Share to MVK gene
Share to Hydroxymethylglutaryl-CoA Reductase Inhibitors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypergammaglobulinemia

Share to Immunoglobulin D

Share to Mutation

Share to Phosphotransferases (Alcohol Group Acceptor)

Share to Syndrome

Source

Identifiers

PMID: 17473510
DOI: 10.2177/jsci.30.86

Genes

MVK

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[MVK gene abnormality and new approach to treatment of hyper IgD syndrome and periodic fever syndrome].PMID 17473510Read ↗

[Mevalonate kinase deficiency in 2016].Semantic proximity Read ↗

[Periodic fever with increased IgD].Semantic proximity Read ↗

Molecular analysis of the mevalonate kinase gene in a cohort of patients with the hyper-igd and periodic fever syndrome: its application as a diagnostic tool.Semantic proximity Read ↗

Hyper-IgD syndrome or mevalonate kinase deficiency.Semantic proximity Read ↗

[Utility of denaturing high performance liquid chromatography (DHPLC) for the diagnosis of mevalonate kinase deficiency in periodic disease].Semantic proximity Read ↗

Mutational spectrum and genotype-phenotype correlations in mevalonate kinase deficiency.Semantic proximity Read ↗

Hyper-IgD syndrome/mevalonate kinase deficiency: what is new?Semantic proximity Read ↗

MVK mutations and associated clinical features in Italian patients affected with autoinflammatory disorders and recurrent fever.Semantic proximity Read ↗

Molecular analysis of MVK mutations and enzymatic activity in hyper-IgD and periodic fever syndrome.Semantic proximity Read ↗

Mevalonate kinase deficiency: an updated clinical overview and revision of the SHARE recommendations.Semantic proximity Read ↗

Mevalonate kinase genotype in children with recurrent fevers and high serum IgD level.Semantic proximity Read ↗

Temperature dependence of mutant mevalonate kinase activity as a pathogenic factor in hyper-IgD and periodic fever syndrome.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.