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Article

[A new auto-inflammatory genetic disease associated with cold urticaria: Plaid involving PLCG2 mutation].

Annales de dermatologie et de venereologie - 1 Nov 2015

Dereure O

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 26149917
DOI: 10.1016/j.annder.2015.05.002

Genes

PLCG2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

[A new auto-inflammatory genetic disease associated with cold urticaria: Plaid involving PLCG2 mutation].PMID 26149917Read ↗

A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency.Semantic proximity Read ↗

A new report of autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (APLAID) with a homozygous pattern from Iran.Semantic proximity Read ↗

[Autoinflammatory disorders: a new concept in hereditary periodic fever syndromes].Semantic proximity Read ↗

PLAID: a Syndrome of Complex Patterns of Disease and Unique Phenotypes.Semantic proximity Read ↗

PLCG2-associated immune dysregulation (PLAID) comprises broad and distinct clinical presentations related to functional classes of genetic variants.Semantic proximity Read ↗

Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle–Wells syndromeSemantic proximity Read ↗

Distinct Cutaneous Manifestations and Cold-Induced Leukocyte Activation Associated With PLCG2 Mutations.Semantic proximity Read ↗

Case Report: A Rare Case of Autoinflammatory Phospholipase Cγ2 (PLCγ2)-Associated Antibody Deficiency and Immune Dysregulation Complicated With Gangrenous Pyoderma and Literature Review.Semantic proximity Read ↗

Overlap of familial Mediterranean fever and autoinflammatory PLCG2-associated antibody deficiency and immune dysregulation in a Turkish patientSemantic proximity Read ↗

Splice site and<i>de novo</i>mutations can cause mixed dominant negative/gain of function<i>PLCG2</i>-associated immune dysregulation with cold urticaria (CU-PLAID)Semantic proximity Read ↗

Splice site and de novo variants can cause PLCG2-associated immune dysregulation with cold urticaria.Semantic proximity Read ↗

Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions.Semantic proximity Read ↗

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