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dc.contributor.authorSag, Erdal
dc.contributor.authorGocmen, Rahsan
dc.contributor.authorYildiz, F. Gokcem
dc.contributor.authorOzturk, Zeynelabidin
dc.contributor.authorTemucin, Cagri
dc.contributor.authorTeksam, Ozlem
dc.contributor.authorUtine, Eda
dc.date.accessioned2019-12-10T10:35:24Z
dc.date.available2019-12-10T10:35:24Z
dc.date.issued2016
dc.identifier.issn0031-4005
dc.identifier.urihttps://doi.org/10.1542/peds.2015-1771
dc.identifier.urihttp://hdl.handle.net/11655/13874
dc.description.abstractCongenital mirror movements are rare conditions that define the inability to perform unimanual movements. Gorlin syndrome, also known as nevoid basal cell carcinoma syndrome, is a genetic disorder with multiple nevi predisposing to basal cell carcinoma, odontogenic keratocysts, and skeletal malformations. Herein we report on an adolescent patient with Gorlin syndrome and coexisting congenital mirror movements. To our knowledge, this is the first patient in the literature who has both of these very rare conditions.
dc.language.isoen
dc.publisherAmer Acad Pediatrics
dc.relation.isversionof10.1542/peds.2015-1771
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectPediatrics
dc.titleCongenital Mirror Movements In Gorlin Syndrome: A Case Report With Dti And Functional Mri Features
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalPediatrics
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume137
dc.identifier.issue3
dc.description.indexWoS
dc.description.indexScopus


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