A novel NFkB1 mutation linking pyoderma gangrenosum and common variable immunodeficiency
Author:
Publisher
Elsevier BV
Subject
Dermatology
Reference10 articles.
1. Pyoderma gangrenosum in a patient with common variable primary immunodeficiency;Bergler-Czop;Postepy Dermatol Alergol,2013
2. The association of age with clinical presentation and comorbidities of pyoderma gangrenosum;Ashchyan;JAMA Dermatol,2018
3. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans;Tuijnenburg;J Allergy Clin Immunol,2018
4. The genetics of pyoderma gangrenosum and implications for treatment: a systematic review;DeFilippis;Br J Dermatol,2015
5. Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes;Kaustio;J Allergy Clin Immunol,2017
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1. Clinical, Immunological, and Genetic Features in Patients with NFKB1 and NFKB2 Mutations: a Systematic Review;Journal of Clinical Immunology;2024-07-11
2. Human Inborn Errors of Immunity in Pyoderma Gangrenosum: A Systematic Review;American Journal of Clinical Dermatology;2024-07-01
3. A novel splice-site mutation in NFKB1 presenting as common variable immunodeficiency and postoperative hyperinflammation responsive to anti–IL-1 therapy;The Journal of Allergy and Clinical Immunology: In Practice;2024-06
4. Truncating NFKB1 variants cause combined NLRP3 inflammasome activation and type I interferon signaling and predispose to necrotizing fasciitis;Cell Reports Medicine;2024-04
5. Genetic mutations in pyoderma gangrenosum, hidradenitis suppurativa, and associated autoinflammatory syndromes: Insights into pathogenic mechanisms and shared pathways;The Journal of Dermatology;2023-11-30
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