Literature DB >> 8750801

Familial idiopathic atrial fibrillation with bradyarrhythmia.

H Bertram1, T Paul, F Beyer, H C Kallfelz.   

Abstract

UNLABELLED: A 10-year-old boy is reported who presented with idiopathic atrial fibrillation and bradyarrhythmia. After history of intrauterine and postnatal bradycardia, atrial fibrillation was first documented electrocardiographically at 16 months of age. An underlying structural heart disease was not evident. At the age of 10 years, implantation of a permanent ventricular demand pacemaker was indicated after syncope due to severe bradyarrhythmia. The family history revealed five persons of four generations with bradyarrhythmias. Idiopathic atrial fibrillation known since childhood was documented in three close relatives. A high grade AV block resulting in bradyarrhythmias and the occurrence of ST-T-changes in precordial leads could be demonstrated in all affected family members suggesting a diffuse general conduction abnormality in these patients. In this family, idiopathic atrial fibrillation seems to be transmitted as an autosomal dominant trait.
CONCLUSION: Atrial fibrillation without underlying heart disease is extremely rare in children. Careful electrocardiographic follow-up of these patients and the evaluation of ECG recordings of all family members is recommended.

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Mesh:

Year:  1996        PMID: 8750801     DOI: 10.1007/bf02115617

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  26 in total

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  5 in total

1.  Familial aggregation in lone atrial fibrillation.

Authors:  Patrick T Ellinor; Danita M Yoerger; Jeremy N Ruskin; Calum A MacRae
Journal:  Hum Genet       Date:  2005-11-15       Impact factor: 4.132

Review 2.  T-type channels in the sino-atrial and atrioventricular pacemaker mechanism.

Authors:  Pietro Mesirca; Angelo G Torrente; Matteo E Mangoni
Journal:  Pflugers Arch       Date:  2014-02-27       Impact factor: 3.657

Review 3.  Genomics of Atrial Fibrillation.

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4.  Pacemaker channel dysfunction in a patient with sinus node disease.

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5.  Cardiac arrhythmia induced by genetic silencing of 'funny' (f) channels is rescued by GIRK4 inactivation.

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Journal:  Nat Commun       Date:  2014-08-21       Impact factor: 14.919

  5 in total

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