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De novo interstitial deletion of 9q32-34.1 with mental retardation, developmental delay, epilepsy, and cortical dysplasia: A case report

dc.contributor.authorTos, Tülay
dc.contributor.authorAlp, Muhammed Yunus
dc.contributor.authorKaracan, Can Demir
dc.contributor.authorAndıran, Nesibe
dc.contributor.authorÇolakoglu, E. Y.
dc.date.accessioned2024-01-23T05:54:28Z
dc.date.available2024-01-23T05:54:28Z
dc.date.issued2014
dc.description.abstractDe novo interstitial deletion of 9q32-34.1 with mental retardation, developmental delay, epilepsy, and cortical dysplasia: a case report: In this report we describe a 10 year-old female patient with interstitial deletion of 9q32-q34.1 associated with mental retardation, developmental delay, short stature, mild facial dysmorphism, epilepsy, abnormal EEG and brain MRI findings consistent with focal cortical dysplasia. Interstitial deletion of 9q associated with q32-q34 is found extremely rare. Common features of seven previously reported cases are mental retardation, developmental delay, short stature, a distinct cranial and facial phenotype (brachycephaly, low midface, low and prominent forehead, and low set malformed ears). Combination of epilepsy, abnormal EEG and brain MRI findings are not reported before.
dc.identifier.citationTos, T. vd. (2014). "De novo interstitial deletion of 9q32-34.1 with mental retardation, developmental delay, epilepsy, and cortical dysplasia: A case report". Genetic Counseling, 25(2), 197-201.
dc.identifier.endpage201
dc.identifier.issn1015-8146
dc.identifier.issue2
dc.identifier.pubmed25059019
dc.identifier.scopus2-s2.0-84904246811
dc.identifier.startpage197
dc.identifier.urihttps://hdl.handle.net/11452/39243
dc.identifier.volume25
dc.identifier.wos000338752600010
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherMedecine Et Hygiene
dc.relation.journalGenetic Counseling
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectCortical dysplasia
dc.subjectMental retardation
dc.subjectDevelopmental delay
dc.subjectInterstitial deletion 9q32-q34.1
dc.subjectEpilepsy
dc.subjectBiotechnology & applied microbiology
dc.subjectGenetics & heredity
dc.subjectResearch & experimental medicine
dc.subjectMedical ethics
dc.subject.emtreeArticle
dc.subject.emtreeCase report
dc.subject.emtreeChild
dc.subject.emtreeChromosome 9q
dc.subject.emtreeChromosome analysis
dc.subject.emtreeCortical dysplasia
dc.subject.emtreeDevelopmental disorder
dc.subject.emtreeElectroencephalogram
dc.subject.emtreeEpilepsy
dc.subject.emtreeFace dysmorphia
dc.subject.emtreeFemale
dc.subject.emtreeGenetic disorder
dc.subject.emtreeHuman
dc.subject.emtreeIntelligence quotient
dc.subject.emtreeInterstitial chromosome deletion
dc.subject.emtreeKaryotype
dc.subject.emtreeLearning disorder
dc.subject.emtreeMental deficiency
dc.subject.emtreeNuclear magnetic resonance imaging
dc.subject.emtreeRare disease
dc.subject.emtreeSchool child
dc.subject.emtreeSecond degree relative
dc.subject.emtreeSpecial education
dc.subject.emtreeStanford-binet intelligence scale
dc.subject.emtreeTemporal lobe
dc.subject.meshChild
dc.subject.meshChromosome deletion
dc.subject.meshChromosomes, human, pair 9
dc.subject.meshDevelopmental disabilities
dc.subject.meshEpilepsy
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshIntellectual disability
dc.subject.meshMalformations of cortical development
dc.subject.scopusBasal Cell Nevus Syndrome; Jaw Cysts; Mutation
dc.subject.wosBiotechnology & applied microbiology
dc.subject.wosMedicine, research & experimental
dc.subject.wosGenetics & heredity
dc.subject.wosMedical ethics
dc.titleDe novo interstitial deletion of 9q32-34.1 with mental retardation, developmental delay, epilepsy, and cortical dysplasia: A case report
dc.typeArticle
dc.wos.quartileQ4
dspace.entity.typePublication
local.indexed.atWOS
local.indexed.atScopus

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