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dc.contributor.authorBolat, Gül Ünsel
dc.date.accessioned2021-03-01T11:05:53Z
dc.date.available2021-03-01T11:05:53Z
dc.date.issued2020en_US
dc.identifier.issn1355-4794
dc.identifier.issn1465-3656
dc.identifier.urihttps://doi.org/10.1080/13554794.2020.1853174
dc.identifier.urihttps://hdl.handle.net/20.500.12462/11104
dc.description.abstractOculocutaneous albinism (OCA) is a group of autosomal recessive disorders characterized by impairment in the melanin synthesis. We report two siblings with OCA who presented with symptoms of autism spectrum disorder and attention deficit hyperactivity disorder (ADHD). Ocular side effects occured after methylphenidate (MPH) treatment in the patient with ADHD and OCA. The diagnosis of OCA has been associated with difficulties in academic and social fields due to decreased visual activity and differentiation of phenotypic characteristics. Delayed diagnosis of comorbid neuropsychiatric disorders and MPH therapy may increase these difficulties. Patients with OCA require careful evaluation and treatment for neuropsychiatric disorders.en_US
dc.language.isoengen_US
dc.publisherRoutledge Journalsen_US
dc.relation.isversionof10.1080/13554794.2020.1853174en_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectASDen_US
dc.subjectADHDen_US
dc.subjectAlbinismen_US
dc.subjectVisual Side Effecten_US
dc.subjectMethylphenidateen_US
dc.titleCase report: diagnosis and treatment of attention deficit hyperactivity disorder and autism spectrum disorder in patients diagnosed with oculocutaneous albinismen_US
dc.typearticleen_US
dc.relation.journalNeurocaseen_US
dc.contributor.departmentTıp Fakültesien_US
dc.contributor.authorID0000-0002-4574-421Xen_US
dc.identifier.volume26en_US
dc.identifier.issue6en_US
dc.identifier.startpage360en_US
dc.identifier.endpage363en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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