Phacomatosis pigmentovascularis type IIB associated with Sturge-Weber syndrome: A case report and review of the literature

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dc.contributor.authorSönmez, Fatma Müjgan
dc.contributor.authorAksoy, Ays?e
dc.contributor.authorSarı, Ahmet
dc.contributor.authorErpolat, Seval
dc.contributor.authorÖzkaya, A. K.
dc.date.accessioned2025-10-24T18:06:52Z
dc.date.available2025-10-24T18:06:52Z
dc.date.issued2013
dc.departmentMalatya Turgut Özal Üniversitesi
dc.description.abstract[No abstract available]
dc.identifier.endpage250
dc.identifier.issn1015-8146
dc.identifier.issue2
dc.identifier.pmid24032298
dc.identifier.scopus2-s2.0-84884338371
dc.identifier.scopusqualityN/A
dc.identifier.startpage247
dc.identifier.urihttps://hdl.handle.net/20.500.12899/3246
dc.identifier.volume24
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.relation.ispartofGenetic Counseling
dc.relation.publicationcategoryDiğer
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzScopus_20251023
dc.subjectphenobarbital
dc.subjectabdominal radiography
dc.subjectbiochemistry
dc.subjectblood cell count
dc.subjectbrain atrophy
dc.subjectbrain calcification
dc.subjectbrain region
dc.subjectbrain tomography
dc.subjectcase report
dc.subjectcongenital glaucoma
dc.subjectcyanosis
dc.subjectdisease association
dc.subjectelectric potential
dc.subjectelectroencephalography
dc.subjectepileptic state
dc.subjectfemale
dc.subjecthemiplegia
dc.subjecthuman
dc.subjectinfant
dc.subjectletter
dc.subjectmagnetic resonance angiography
dc.subjectmental deficiency
dc.subjectmotor retardation
dc.subjectneuroimaging
dc.subjectnevus flammeus
dc.subjectnuclear magnetic resonance imaging
dc.subjectphacomatosis pigmentovascularis type IIb
dc.subjectphakomatosis
dc.subjectphysical examination
dc.subjectposterior cerebral artery
dc.subjectright hemisphere
dc.subjectseizure
dc.subjectskin defect
dc.subjectSturge Weber syndrome
dc.subjectthorax radiography
dc.subjectAtrophy
dc.subjectChild
dc.subjectDevelopmental Disabilities
dc.subjectFemale
dc.subjectHumans
dc.subjectIntellectual Disability
dc.subjectNeurocutaneous Syndromes
dc.subjectStatus Epilepticus
dc.subjectSturge-Weber Syndrome
dc.titlePhacomatosis pigmentovascularis type IIB associated with Sturge-Weber syndrome: A case report and review of the literature
dc.typeLetter

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