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

PAPA-like syndrome with heterozygous mutation in the MEFV gene.

Clinical and experimental dermatology - 1 Mar 2022

O'Connor C, Kiely L, Heffron C, Ryan J, Bennett M

Abstract excerpt

A patient presented with a history of recurrent pyoderma gangrenosum, arthritis and extensive acne, prompting a genetic workup for PAPA syndrome. An MEFV mutation was identified and a change in therapeutic strategy from anakinra to colchicine was successful. Click https://www.wileyhealthlearning.com/#/online-courses/b52447c0-1d37-472d-b0c0-7817352d6f68 for the corresponding questions to this CME article.

Read the complete abstract on PubMed

Topics

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

Share to Acne Vulgaris
Share to Arthritis, Infectious
Share to Cicatrix

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Colchicine

Share to Muscular Atrophy

Share to Recurrence

Share to Tubulin Modulators

Source

Identifiers

PMID: 34882829
DOI: 10.1111/ced.15027

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PAPA-like syndrome with heterozygous mutation in the MEFV gene.PMID 34882829Read ↗

A heterozygous variant in MEFV in a familial autoinflammatory syndrome with PAPA-like featuresSemantic proximity Read ↗

PAPASH syndrome with MEFV gene mutation.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 ↗

[Still disease with heterozygous MEFV mutation].Semantic proximity Read ↗

P03-005 - MEFV heterozygous mutations in PFAPA patientsSemantic proximity Read ↗

Expanding clinical spectrum of autosomal dominant pyrin-associated autoinflammatory disorder caused by the heterozygous MEFV p.Thr577Asn variant.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 ↗

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

Successful treatment with anakinra in generalized spiculated porokeratosis and severe hidradenitis suppurativa in a patient with MVK and MEFV mutations.Semantic proximity Read ↗

A case of familial Mediterranean fever with triple MEFV gene mutations.Semantic proximity Read ↗

Could familial Mediterranean fever gene mutations be related to PFAPA syndrome?Semantic proximity Read ↗

MEFV gene mutation in two cases of pyoderma gangrenosum with aseptic arthritis.Semantic proximity Read ↗

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