Tumor Necrosis Factor Receptor-associated Periodic Syndrome
What's New
Last Posted: Jan 05, 2023
- Diagnostic and therapeutic algorithms for monogenic autoinflammatory diseases presenting with recurrent fevers among adults.
Delplanque Marion et al. Rheumatology (Oxford, England) 2022 - Diagnostic Rate of Autoinflammatory Diseases Evaluated by Fever Patterns in Pediatric- and Adult-Onset Patients.
Miyamae Takako, et al. Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases 2020 3 (2) 60-62 - The Heart Matters: Contribution of Genetic Factors in Recurrent Pericarditis.
Perricone Carlo et al. The Israel Medical Association journal : IMAJ 2019 Jul 21(7) 487-490 - Novel presentations of periodic fever syndromes: Discrepancies between genetic and clinical diagnoses.
Hoang Tiffany K et al. European journal of rheumatology 2018 Nov 1-7 - The patient journey to diagnosis and treatment of autoinflammatory diseases.
Hausmann Jonathan S et al. Orphanet journal of rare diseases 2018 Sep 13(1) 156 - A Comprehensive Overview of the Hereditary Periodic Fever Syndromes.
Rigante Donato et al. Clinical reviews in allergy & immunology 2016 Apr - Adult autoinflammatory disease frequency and our diagnostic experience in an adult autoinflammatory clinic.
Yao Qingping, et al. Seminars in arthritis and rheumatism 2015 10 - Performance of Different Diagnostic Criteria for Familial Mediterranean Fever in Children with Periodic Fevers: Results from a Multicenter International Registry.
Demirkaya Erkan et al. The Journal of rheumatology 2015 Nov - TNFRSF1A Gene Causing Tumor Necrosis Factor Receptor-associated Periodic Syndrome in 2 Siblings Displaying Variable Disease Severity and Discordant Heterozygosity for an MEFV E148Q Variant.
Abdwani Reem, et al. The Journal of rheumatology 2015 8 (8) 1534-5 - Clues to detect tumor necrosis factor receptor-associated periodic syndrome (TRAPS) among patients with idiopathic recurrent acute pericarditis: results of a multicentre study.
Cantarini L, et al. Clinical research in cardiology : official journal of the German Cardiac Society 2012 2
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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