Screening, diagnosis and follow-up of Brugada syndrome in children:a Dutch expert consensus statement

Brugada syndrome (BrS) is a rare inherited arrhythmia syndrome. Affected children may experience life-threatening symptoms, mainly during fever. The percentage of SCN5A variant carriers in children is higher than in adults. Current diagnostic and follow-up policies for children with (a family history of) BrS vary between centres. Here, we present a consensus statement based on the current literature and expert opinions to standardise the approach for all children with BrS and those from BrS families in the Netherlands. In summary, BrS is diagnosed in patients with a spontaneous type 1 electroc... Mehr ...

Verfasser: Peltenburg, P. J.
Hoedemaekers, Y. M.
Clur, S. A. B.
Blom, N. A.
Blank, A. C.
Boesaard, E. P.
Frerich, S.
van den Heuvel, F.
Wilde, A. A. M.
Kammeraad, J. A. E.
Dokumenttyp: Artikel
Erscheinungsdatum: 2023
Reihe/Periodikum: Peltenburg , P J , Hoedemaekers , Y M , Clur , S A B , Blom , N A , Blank , A C , Boesaard , E P , Frerich , S , van den Heuvel , F , Wilde , A A M & Kammeraad , J A E 2023 , ' Screening, diagnosis and follow-up of Brugada syndrome in children : a Dutch expert consensus statement ' , Netherlands Heart Journal , pp. 133–137 . https://doi.org/10.1007/s12471-022-01723-6
Schlagwörter: Brugada syndrome / DNA diagnostics / Family screening / Follow-up / Children / RISK STRATIFICATION / CLINICAL-FEATURES / YOUNG-PATIENTS / MANAGEMENT
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26672223
Datenquelle: BASE; Originalkatalog
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Link(s) : https://hdl.handle.net/11370/fab517fb-63e7-422a-a55b-0bdb2f8cd162