Diagnostic challenge of hyper-IgD syndrome in four children with inflammatory gastrointestinal complaints
Author:
Publisher
Informa UK Limited
Subject
Gastroenterology
Link
http://www.tandfonline.com/doi/pdf/10.1080/00365520500327743
Reference32 articles.
1. Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome
2. Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome
3. Lack of isoprenoid products raises ex vivo interleukin-1? secretion in hyperimmunoglobulinemia D and periodic fever syndrome
4. Hyperimmunoglobulinemia D and Periodic Fever Syndrome
5. Mevalonate kinase deficiency in a child with periodic fever and without hyperimmunoglobulinaemia D
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1. The 2021 EULAR/American College of Rheumatology points to consider for diagnosis, management and monitoring of the interleukin-1 mediated autoinflammatory diseases: cryopyrin-associated periodic syndromes, tumour necrosis factor receptor-associated periodic syndrome, mevalonate kinase deficiency, and deficiency of the interleukin-1 receptor antagonist;Annals of the Rheumatic Diseases;2022-05-27
2. The 2021 EULAR/American College of Rheumatology Points to Consider for Diagnosis, Management and Monitoring of the Interleukin‐1 Mediated Autoinflammatory Diseases: Cryopyrin‐Associated Periodic Syndromes, Tumour Necrosis Factor Receptor‐Associated Periodic Syndrome, Mevalonate Kinase Deficiency, and Deficiency of the Interleukin‐1 Receptor Antagonist;Arthritis & Rheumatology;2022-05-27
3. Teleost IgD+IgM− B Cells Mount Clonally Expanded and Mildly Mutated Intestinal IgD Responses in the Absence of Lymphoid Follicles;Cell Reports;2019-12
4. Omics technologies and the choice of treatment strategy for inflammatory intestinal diseases;Dokazatel'naya gastroenterologiya;2018
5. Ultrasonographic findings in hyperimmunoglobulin D syndrome: a case report;Medical Ultrasonography;2017-04-22
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