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Carpenter Syndrome: Report of Two Siblings

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dc.authorscopusid7003707808
dc.authorscopusid7003539720
dc.authorscopusid7004140928
dc.authorscopusid7003692769
dc.authorscopusid6701723040
dc.contributor.authorİşlek, I.
dc.contributor.authorKüçüködük, S.
dc.contributor.authorIncesu, L.
dc.contributor.authorSelçuk, M.B.
dc.contributor.authorAygün, D.
dc.date.accessioned2020-06-21T15:53:05Z
dc.date.available2020-06-21T15:53:05Z
dc.date.issued1998
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[İşlek] İsmail, Department of Pediatrics, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Department of Pediatrics, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Küçüködük] Şükrü, Department of Pediatrics, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Incesu] Lütfi, Department of Radiology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Selçuk] Mustafa Bekir, Department of Radiology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Aygün] Dursun, Department of Neurology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractCarpenter syndrome consists of acrocephaly, soft tissue syndactyly, short fingers, preaxial polydactyly, congenital heart disease, hypogenitalism, cryptorchidism, obesity, umbilical hernia and mental retardation. Here we report two affected sibs (IQs were 80 and 93) presenting various cerebrospinal malformations, ie frontal lobe deformity, narrowed foramen magnum, hypoplastic posterior fossa, kinked spinal cord, and syrinx cavitation demonstrated by magnetic resonance imaging.en_US
dc.identifier.doi10.1097/00019605-199807000-00005
dc.identifier.endpage189en_US
dc.identifier.issn0962-8827
dc.identifier.issn1473-5717
dc.identifier.issue3en_US
dc.identifier.pmid9689991
dc.identifier.scopus2-s2.0-0031851733
dc.identifier.scopusqualityQ4
dc.identifier.startpage185en_US
dc.identifier.urihttps://doi.org/10.1097/00019605-199807000-00005
dc.identifier.volume7en_US
dc.identifier.wosWOS:000074640200005
dc.identifier.wosqualityQ4
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.ispartofClinical Dysmorphologyen_US
dc.relation.journalClinical Dysmorphologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAcrocephalopolysyndactylyen_US
dc.subjectCarpenter Syndromeen_US
dc.subjectCerebrospinal Malformationsen_US
dc.titleCarpenter Syndrome: Report of Two Siblingsen_US
dc.typeArticleen_US
dspace.entity.typePublication

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