Validation of the new classification criteria for hereditary recurrent fever in an independent cohort: experience from the JIR Cohort Database.

Dingulu, Glory; Georgin-Lavialle, Sophie; Koné-Paut, Isabelle; Pillet, Pascal; Pagnier, Anne; Merlin, Etienne; Kaiser, Daniela; Belot, Alexandre; Hofer, Michael; Hentgen, Véronique

Dingulu, Glory; Georgin-Lavialle, Sophie; Koné-Paut, Isabelle; Pillet, Pascal; Pagnier, Anne; Merlin, Etienne; Kaiser, Daniela; Belot, Alexandre; Hofer, Michael; Hentgen, Véronique.

Affiliation

Dingulu G; National Referral Centre of Auto-Inflammatory Diseases and Inflammatory Amyloidosis, - CEREMAIA, Department of Pediatrics, Versailles Hospital, Le Chesnay.
Georgin-Lavialle S; Service de Médecine Interne-CEREMAIA, Centre Hospitalier Universitaire Tenon, Paris.
Koné-Paut I; Service de Rhumatologie Pédiatrique-CEREMAIA, Centre Hospitalier Universitaire Le Kremlin Bicêtre, APHP, Université de Paris sud Saclay, Le Kremlin Bicêtre.
Pillet P; Service d'Accueil des Urgences Pédiatriques, Centre Hospitalier Universitaire Pellegrin, Bordeaux.
Pagnier A; Service de d'Hémato-oncologie Pédiatrique, Centre Hospitalier Universitaire de Grenoble, France.
Merlin E; Service de Pédiatrie Générale, Centre Hospitalier Universitaire Clermont Ferrand, Clermont Ferrand.
Kaiser D; Centre Hospitalier Cantonal Luzern, Service de Pédiatrie Générale, Luzern.
Belot A; Service de Néphrologie, Rhumatologie, Dermatologie Pédiatrique, Hôpital Femme Mère, Enfant, Hospices Civils de Lyon, Université de Lyon, Lyon.
Hofer M; Service de Rhumatologie Pédiatrique, Centre Hospitalier Universitaire Vaudois, Lausanne, France.
Hentgen V; National Referral Centre of Auto-Inflammatory Diseases and Inflammatory Amyloidosis, - CEREMAIA, Department of Pediatrics, Versailles Hospital, Le Chesnay.

Rheumatology (Oxford) ; 59(10): 2947-2952, 2020 Oct 01.

Article in En | MEDLINE | ID: mdl-32125423

Subject(s)

Hereditary Autoinflammatory Diseases/classification; Cohort Studies; Cryopyrin-Associated Periodic Syndromes/classification; Cryopyrin-Associated Periodic Syndromes/genetics; Databases, Factual; Familial Mediterranean Fever/classification; Familial Mediterranean Fever/genetics; Genotype; Hereditary Autoinflammatory Diseases/genetics; Humans; Lymphadenitis/genetics; Mevalonate Kinase Deficiency/classification; Mevalonate Kinase Deficiency/genetics; Mutation; Pharyngitis/genetics; Sensitivity and Specificity; Stomatitis, Aphthous/genetics; Syndrome

Key words

TNF-α; classification criteria; cryopyrin-associated periodic syndrome; familial Mediterranean fever; hereditary recurrent fever; mevalonate kinase deficiency; receptor-associated periodic syndrome

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hereditary Autoinflammatory Diseases Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Humans Language: En Journal: Rheumatology (Oxford) Journal subject: REUMATOLOGIA Year: 2020 Type: Article

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