Epilepsy and Spinocerebellar Ataxia

A large consanguinous family from Saudi Arabia with 4 affected children presenting with an autosomal recessive ataxia, generalized tonic-clonic epilepsy and mental retardation is reported from the Institut de Genetique, Universite Louis Pasteur, Illkirch, France; Division of Pediatric Neurology, Kin...

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Main Author: J Gordon Millichap
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 2007-07-01
Series:Pediatric Neurology Briefs
Subjects:
Online Access:https://www.pediatricneurologybriefs.com/articles/1013
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spelling doaj-bdbff860dedb4b2f92741c92bf360a212020-11-25T02:38:44ZengPediatric Neurology Briefs PublishersPediatric Neurology Briefs1043-31552166-64822007-07-01217535410.15844/pedneurbriefs-21-7-6999Epilepsy and Spinocerebellar AtaxiaJ Gordon Millichap0Northwestern University Feinberg School of MedicineA large consanguinous family from Saudi Arabia with 4 affected children presenting with an autosomal recessive ataxia, generalized tonic-clonic epilepsy and mental retardation is reported from the Institut de Genetique, Universite Louis Pasteur, Illkirch, France; Division of Pediatric Neurology, King Saud University, Riyadh, Saudi Arabia; and other centers.https://www.pediatricneurologybriefs.com/articles/1013spinocerebellar ataxiacerebellar vermis atrophymyoclonic epilepsy with ragged red fibers
collection DOAJ
language English
format Article
sources DOAJ
author J Gordon Millichap
spellingShingle J Gordon Millichap
Epilepsy and Spinocerebellar Ataxia
Pediatric Neurology Briefs
spinocerebellar ataxia
cerebellar vermis atrophy
myoclonic epilepsy with ragged red fibers
author_facet J Gordon Millichap
author_sort J Gordon Millichap
title Epilepsy and Spinocerebellar Ataxia
title_short Epilepsy and Spinocerebellar Ataxia
title_full Epilepsy and Spinocerebellar Ataxia
title_fullStr Epilepsy and Spinocerebellar Ataxia
title_full_unstemmed Epilepsy and Spinocerebellar Ataxia
title_sort epilepsy and spinocerebellar ataxia
publisher Pediatric Neurology Briefs Publishers
series Pediatric Neurology Briefs
issn 1043-3155
2166-6482
publishDate 2007-07-01
description A large consanguinous family from Saudi Arabia with 4 affected children presenting with an autosomal recessive ataxia, generalized tonic-clonic epilepsy and mental retardation is reported from the Institut de Genetique, Universite Louis Pasteur, Illkirch, France; Division of Pediatric Neurology, King Saud University, Riyadh, Saudi Arabia; and other centers.
topic spinocerebellar ataxia
cerebellar vermis atrophy
myoclonic epilepsy with ragged red fibers
url https://www.pediatricneurologybriefs.com/articles/1013
work_keys_str_mv AT jgordonmillichap epilepsyandspinocerebellarataxia
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