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Periodic fever syndromes in Eastern and Central European countries: results of a pediatric multinational survey

OBJECTIVE: To analyze the prevalence of diagnosed and suspected autoinflammatory diseases in Eastern and Central European (ECE) countries, with a particular interest on the diagnostic facilities in these countries. METHODS: Two different strategies were used to collect data on patients with periodic...

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Autores principales: Toplak, Nataša, Dolezalovà, Pavla, Constantin, Tamas, Sedivà, Anna, Pašić, Srdjan, Čižnar, Peter, Wolska-Kuśnierz, Beata, Harjaček, Miroslav, Stefan, Mariana, Ruperto, Nicolino, Gattorno, Marco, Avčin, Tadej
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3014922/
https://www.ncbi.nlm.nih.gov/pubmed/21539753
http://dx.doi.org/10.1186/1546-0096-8-29
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author Toplak, Nataša
Dolezalovà, Pavla
Constantin, Tamas
Sedivà, Anna
Pašić, Srdjan
Čižnar, Peter
Wolska-Kuśnierz, Beata
Harjaček, Miroslav
Stefan, Mariana
Ruperto, Nicolino
Gattorno, Marco
Avčin, Tadej
author_facet Toplak, Nataša
Dolezalovà, Pavla
Constantin, Tamas
Sedivà, Anna
Pašić, Srdjan
Čižnar, Peter
Wolska-Kuśnierz, Beata
Harjaček, Miroslav
Stefan, Mariana
Ruperto, Nicolino
Gattorno, Marco
Avčin, Tadej
author_sort Toplak, Nataša
collection PubMed
description OBJECTIVE: To analyze the prevalence of diagnosed and suspected autoinflammatory diseases in Eastern and Central European (ECE) countries, with a particular interest on the diagnostic facilities in these countries. METHODS: Two different strategies were used to collect data on patients with periodic fever syndromes from ECE countries- the Eurofever survey and collection of data with the structured questionnaire. RESULTS: Data from 35 centers in 14 ECE countries were collected. All together there were 11 patients reported with genetically confirmed familial Mediterranean fever (FMF), 14 with mevalonate-kinase deficiency (MKD), 11 with tumor necrosis factor receptor associated periodic syndrome (TRAPS) and 4 with chronic infantile neurological cutaneous and articular syndrome (CINCA). Significantly higher numbers were reported for suspected cases which were not genetically tested. All together there were 49 suspected FMF patients reported, 24 MKD, 16 TRAPS, 7 CINCA and 2 suspected Muckle-Wells syndrome (MWS) patients. CONCLUSIONS: The number of genetically confirmed patients with periodic fever syndromes in ECE countries is very low. In order to identify more patients in the future, it is important to organize educational programs for increasing the knowledge on these diseases and to establish a network for genetic testing of periodic fever syndromes in ECE countries.
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spelling pubmed-30149222011-01-05 Periodic fever syndromes in Eastern and Central European countries: results of a pediatric multinational survey Toplak, Nataša Dolezalovà, Pavla Constantin, Tamas Sedivà, Anna Pašić, Srdjan Čižnar, Peter Wolska-Kuśnierz, Beata Harjaček, Miroslav Stefan, Mariana Ruperto, Nicolino Gattorno, Marco Avčin, Tadej Pediatr Rheumatol Online J Short Report OBJECTIVE: To analyze the prevalence of diagnosed and suspected autoinflammatory diseases in Eastern and Central European (ECE) countries, with a particular interest on the diagnostic facilities in these countries. METHODS: Two different strategies were used to collect data on patients with periodic fever syndromes from ECE countries- the Eurofever survey and collection of data with the structured questionnaire. RESULTS: Data from 35 centers in 14 ECE countries were collected. All together there were 11 patients reported with genetically confirmed familial Mediterranean fever (FMF), 14 with mevalonate-kinase deficiency (MKD), 11 with tumor necrosis factor receptor associated periodic syndrome (TRAPS) and 4 with chronic infantile neurological cutaneous and articular syndrome (CINCA). Significantly higher numbers were reported for suspected cases which were not genetically tested. All together there were 49 suspected FMF patients reported, 24 MKD, 16 TRAPS, 7 CINCA and 2 suspected Muckle-Wells syndrome (MWS) patients. CONCLUSIONS: The number of genetically confirmed patients with periodic fever syndromes in ECE countries is very low. In order to identify more patients in the future, it is important to organize educational programs for increasing the knowledge on these diseases and to establish a network for genetic testing of periodic fever syndromes in ECE countries. BioMed Central 2010-12-02 /pmc/articles/PMC3014922/ /pubmed/21539753 http://dx.doi.org/10.1186/1546-0096-8-29 Text en Copyright ©2010 Toplak et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Toplak, Nataša
Dolezalovà, Pavla
Constantin, Tamas
Sedivà, Anna
Pašić, Srdjan
Čižnar, Peter
Wolska-Kuśnierz, Beata
Harjaček, Miroslav
Stefan, Mariana
Ruperto, Nicolino
Gattorno, Marco
Avčin, Tadej
Periodic fever syndromes in Eastern and Central European countries: results of a pediatric multinational survey
title Periodic fever syndromes in Eastern and Central European countries: results of a pediatric multinational survey
title_full Periodic fever syndromes in Eastern and Central European countries: results of a pediatric multinational survey
title_fullStr Periodic fever syndromes in Eastern and Central European countries: results of a pediatric multinational survey
title_full_unstemmed Periodic fever syndromes in Eastern and Central European countries: results of a pediatric multinational survey
title_short Periodic fever syndromes in Eastern and Central European countries: results of a pediatric multinational survey
title_sort periodic fever syndromes in eastern and central european countries: results of a pediatric multinational survey
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3014922/
https://www.ncbi.nlm.nih.gov/pubmed/21539753
http://dx.doi.org/10.1186/1546-0096-8-29
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