Document Detail


Benign familial neonatal convulsions.
MedLine Citation:
PMID:  6412579     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A pedigree of so-called benign familial neonatal convulsions was reported. Nine members experienced convulsions in the neonatal period and/or in early infancy. All members except one had good prognosis. One member had mild mental retardation and epilepsy with rolandic EEG foci. It was suggested that some common genetic factors may be involved in the etiology of benign familial neonatal convulsions, convulsions of unknown etiology in infancy (Fukuyama) and epilepsy with rolandic EEG foci. A review of literature revealed that about 14% of cases with benign familial neonatal convulsions eventually developed epilepsy.
Authors:
Y Takebe; C Chiba; S Kimura
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Brain & development     Volume:  5     ISSN:  0387-7604     ISO Abbreviation:  Brain Dev.     Publication Date:  1983  
Date Detail:
Created Date:  1983-10-08     Completed Date:  1983-10-08     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7909235     Medline TA:  Brain Dev     Country:  JAPAN    
Other Details:
Languages:  eng     Pagination:  319-22     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Anticonvulsants / therapeutic use
Child
Child, Preschool
Electroencephalography
Epilepsies, Partial / genetics
Female
Humans
Infant
Infant, Newborn
Male
Mental Retardation / genetics
Pedigree
Prognosis
Spasms, Infantile / drug therapy,  genetics*
Chemical
Reg. No./Substance:
0/Anticonvulsants

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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