Literature DB >> 6475877

A family history of seizures associated with sudden cardiac deaths.

J T Bricker, A Garson, P C Gillette.   

Abstract

Hereditary prolongation of the Q-T interval is associated with ventricular dysrhythmias. Children with hereditary prolongation of the Q-T interval may have symptoms that seem related to a neurologic abnormality. Two families had members who had been treated with phenytoin sodium for seizures and had died suddenly when the medication was discontinued. Children in both families were found to have prolongation of the Q-T interval. A history of seizures or of seizures in the family may be an indication of hereditary prolongation of the Q-T interval.

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Year:  1984        PMID: 6475877     DOI: 10.1001/archpedi.1984.02140470064021

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  5 in total

Review 1.  Contributions of the Texas Children's Hospital Pediatric Cardiology Program to the field of pediatric cardiology.

Authors:  J T Bricker
Journal:  Tex Heart Inst J       Date:  1997

Review 2.  Molecular genetic aspects of the Romano-Ward long QT syndrome.

Authors:  J A Towbin
Journal:  Tex Heart Inst J       Date:  1994

Review 3.  Current approaches to the clinical assessment of syncope in pediatric population.

Authors:  Ayşe Kaçar Bayram; Ozge Pamukcu; Huseyin Per
Journal:  Childs Nerv Syst       Date:  2016-01-05       Impact factor: 1.475

4.  Familial ventricular tachycardia: a report of four families.

Authors:  C Wren; E Rowland; J Burn; R W Campbell
Journal:  Br Heart J       Date:  1990-03

Review 5.  Cardiovascular manifestations of autonomic epilepsy.

Authors:  Roy Freeman
Journal:  Clin Auton Res       Date:  2006-02       Impact factor: 4.435

  5 in total

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