Periodic Fever, Aphthous Stomatitis, Pharyngitis And Adenitis
What's New
Last Posted: Sep 15, 2023
- Utility of a targeted next-generation sequencing-based genetic screening panel in patients with periodic fever, aphthous stomatitis, pharyngitis, and adenitis syndrome.
Rabia Miray K??la Ekinci, et al. Archives of rheumatology 2023 0 (2) 299-306 - Evaluation of common NLRP3 Q703K variant in pediatric patients with autoinflammatory disease: CAPS and PFAPA.
Yasemin Kendir-Demirkol, et al. The Turkish journal of pediatrics 2023 0 (4) 650-660 - Phenotypes and genotypes of Chinese adult patients with systemic autoinflammatory diseases.
Hua Yichao, et al. Seminars in arthritis and rheumatism 2019 0 (3) 446-452 - The role of Mediterranean fever gene variants in patients with periodic fever, aphthous stomatitis, pharyngitis, and adenitis syndrome.
Yildiz Mehmet, et al. European journal of pediatrics 2020 0 (4) 1051-1058 - Common genetic susceptibility loci link PFAPA syndrome, Behçet's disease, and recurrent aphthous stomatitis.
Manthiram Kalpana, et al. Proceedings of the National Academy of Sciences of the United States of America 2020 0 (25) 14405-14411 - Does having MEFV gene sequence variants affect the clinical course and colchicine response in children with PFAPA syndrome?
Otar Yener Gülçin, et al. European journal of pediatrics 2022 0 (1) 411-417 - Colchicine versus cimetidine: the better choice for Periodic fever, aphthous stomatitis, pharyngitis, adenitis (PFAPA) syndrome prophylaxis, and the role of MEFV gene mutations.
Raeeskarami Seyed Reza, et al. Pediatric rheumatology online journal 2022 0 (1) 72 - Elevated immunoglobulin D levels in children with PFAPA syndrome.
Kovacs Laszlo, et al. Neuro endocrinology letters 2011 0 (6) 743-6 - NLRP3 gene variants and serum NLRP3 levels in periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA) syndrome.
Kaynak Damla, et al. Clinical rheumatology 2022 9 - The rs13075270 and rs13092160 polymorphisms of CCR1 and CCR3 genes on oral aphthous-like lesions in PFAPA syndrome.
Li Weiwei, et al. Cellular and molecular biology (Noisy-le-Grand, France) 2022 1 (4) 328-333
More
About Rare Diseases PHGKB
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
- Content source: