Literature DB >> 7116243

Benign familial neonatal convulsions.

O Dobrescu, A Larbrisseau.   

Abstract

Benign familial neonatal convulsions are a rare genetic seizure disorder inherited as an autosomal dominant trait. They consist of brief episodes of seizures, recurring during the first few days or weeks of life in otherwise normal babies; their prognosis is good. We report a family in which at least 12 members in three generations presented with this condition; they all had an excellent outcome.

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Year:  1982        PMID: 7116243     DOI: 10.1017/s0317167100044188

Source DB:  PubMed          Journal:  Can J Neurol Sci        ISSN: 0317-1671            Impact factor:   2.104


  2 in total

1.  Search for alpha4 and alpha7 nicotinic acetylcholine receptor markers in a pedigree of benign familial infantile convulsions (BFIC).

Authors:  M B Rauschemberger; C Vecchi; F J Barrantes
Journal:  Neurochem Res       Date:  2002-11       Impact factor: 3.996

2.  Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8q.

Authors:  T B Lewis; R J Leach; K Ward; P O'Connell; S G Ryan
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

  2 in total

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