Document Detail


Inheritance of reading epilepsy.
MedLine Citation:
PMID:  810738     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Primary reading epilepsy was diagnosed by special electroencephalographic (EEG) studies in an adolescent youth after his first grand mal seizure. Similar studies of members in three generations of his family showed primary reading epilepsy in his first cousin and in two of his siblings. The disorder in the siblings had not been noticed by parents or teachers and probably would have remained undetected without the use of special techniques. This pedigree buttresses other reported evidence for autosomal dominant transmission of reading epilepsy. The centrencephalic EEG trait also is present in some members of this family. The possible inplications of this association are discussed.
Authors:
R F Daly; F M Forster
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Publication Detail:
Type:  Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Neurology     Volume:  25     ISSN:  0028-3878     ISO Abbreviation:  Neurology     Publication Date:  1975 Nov 
Date Detail:
Created Date:  1976-02-02     Completed Date:  1976-02-02     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0401060     Medline TA:  Neurology     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  1051-4     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Chromosome Aberrations
Chromosome Disorders
Epilepsy, Tonic-Clonic / genetics*
Female
Genes, Dominant
Humans
Male
Pedigree
Reading*

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


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