Publication:
Corticospinal tract involvement in a patient with 3-HMG coenzyme A lyase deficiency

dc.contributor.authorEKİNCİ, GAZANFER
dc.contributor.authorsYylmaz, Yuksel; Ozdemir, Nihal; Ekinci, Gazanfer; Baykal, Tolunay; Kocaman, Canan
dc.date.accessioned2022-03-12T17:19:57Z
dc.date.available2022-03-12T17:19:57Z
dc.date.issued2006
dc.description.abstract3-Hydroxy-3-methylglutaryl coenzyme A lyase deficiency, an inborn error of ketone body synthesis and leucine degradation, is a rare disorder. There are few reports demonstrating clinical and neuroradiologic findings of this condition. This report describes a 3.5-year-old previously healthy male who was admitted with complex partial seizures and was diagnosed as having 3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency. The patient's previous medical history was unremarkable. His development and neurologic examination were normal. Cranial magnetic resonance imaging indicated prominent corticospinal tract and pontine involvement with focal cerebral white matter changes which have not been described in the literature before. (c) 2006 by Elsevier Inc. All rights reserved.
dc.identifier.doi10.1016/j.pediatrneurol.2006.01.009
dc.identifier.issn0887-8994
dc.identifier.pubmed16876013
dc.identifier.urihttps://hdl.handle.net/11424/228176
dc.identifier.wosWOS:000239697900012
dc.language.isoeng
dc.publisherELSEVIER SCIENCE INC
dc.relation.ispartofPEDIATRIC NEUROLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectSYRUP-URINE-DISEASE
dc.subjectCEREBRAL-CORTEX
dc.subjectYOUNG-RATS
dc.subjectLEUCINE
dc.subject3-HYDROXY-3-METHYLGLUTARYL-COENZYME
dc.subjectMRI
dc.titleCorticospinal tract involvement in a patient with 3-HMG coenzyme A lyase deficiency
dc.typearticle
dspace.entity.typePublication
local.avesis.id28afb03f-0e87-4289-8743-b72ee838fc53
local.import.packageSS17
local.indexed.atWOS
local.indexed.atSCOPUS
local.indexed.atPUBMED
local.journal.numberofpages3
oaire.citation.endPage141
oaire.citation.issue2
oaire.citation.startPage139
oaire.citation.titlePEDIATRIC NEUROLOGY
oaire.citation.volume35
relation.isAuthorOfPublication0e0e14ee-3c58-457f-8b29-cae606bb7fc4
relation.isAuthorOfPublication.latestForDiscovery0e0e14ee-3c58-457f-8b29-cae606bb7fc4

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