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

Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case–control study

29 Nov 2018

Abstract excerpt

BACKGROUND: Hidradenitis suppurativa (HS) is a rare, debilitating neutrophilic dermatosis characterized by chronic inflammation of hair follicles. Many inflammatory conditions may accompany HS. OBJECTIVES: To investigate the association of variants of the MEFV gene with a complex HS phenotype. METHODS: Firstly, we identified the clinical characteristics of 119 patients with HS with a complex phenotype (Hurley...

Read the complete abstract on PubMed

Topics

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

Share to Hidradenitis Suppurativa and Treatments
Share to Inflammasome and immune disorders
Share to Streptococcal Infections and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 30488432
DOI: 10.1111/bjd.17466

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case–control studyPMID 30488432Read ↗

Pyrin-associated autoinflammation with neutrophilic dermatosis: A case report.Semantic proximity Read ↗

Hidradenitis suppurativa associated with chromosomal abnormalities, genodermatoses and genetic disorders: a review.Semantic proximity Read ↗

Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance.Semantic proximity Read ↗

Pyrin-associated autoinflammation with neutrophilic dermatosis related to heterozygous MEFV gene variants in cis: Two case reports in a family.Semantic proximity Read ↗

Familial Mediterranean fever patients with hidradenitis suppurativa.Semantic proximity Read ↗

Unravelling the complex pathogenesis of hidradenitis suppurativa.Semantic proximity Read ↗

Hidradenitis Suppurativa: A Perspective on Genetic Factors Involved in the DiseaseSemantic proximity Read ↗

New Diseases Linked to MEFV Variants or Pyrinopathies.Semantic proximity Read ↗

Familial Mediterranean Fever: Recent Developments in Pathogenesis and New Recommendations for ManagementSemantic proximity Read ↗

Complexity in unclassified auto-inflammatory disease: a case report illustrating the potential for disease arising from the allelic burden of multiple variants.Semantic proximity Read ↗

Leveraging genotypes and phenotypes to implement precision medicine in hidradenitis suppurativa management.Semantic proximity Read ↗

A novel Pyrin-Associated Autoinflammation with Neutrophilic Dermatosis mutation further defines 14-3-3 binding of pyrin and distinction to Familial Mediterranean Fever.Semantic proximity Read ↗

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