Arthrogryposis multiplex congenita, epileptic seizures and cortical dysplasia: a case report

dc.contributor.authorViteva, E.
dc.date.accessioned2015-08-07T12:27:02Z
dc.date.available2015-08-07T12:27:02Z
dc.date.issued2013-09
dc.descriptionAddress for correspondence: Dr. Ekaterina Viteva, PhD.; University of Medicine – Plovdiv; Department of Neurology; 15A Vasil Aprilov St.; 4002 Plovdiv, Bulgaria; mobile: +359887752235 ; e-mail: eiviteva@abv.bgen_US
dc.description.abstractSummary. We have presented a case of a 22-year-old patient having a rare variety of arthrogryposis multiplex congenita - arthrogryposis with epileptic seizures and defect in neural migration. We have described the patient’s disease history, the clinical, and laboratory data by giving prominence to the lack of mental retardation and the late onset of the generalized tonic-clonic seizures, despite the present cortical dysplasia. We have also discussed cases reported by other investigators. We consider that our case report is a contribution to the knowledge about the clinical manifestations, the possible results from neuroimaging and electrophysiological methods, and the progression of arthrogryposis multiplex congenita.en_US
dc.identifier.citationE. Viteva. Arthrogryposis multiplex congenita, epileptic seizures and cortical dysplasia: a case report - Acta medica bulgarica , 40, 2013, No 2, 29-32.en_US
dc.identifier.issn0324-1750
dc.identifier.urihttp://hdl.handle.net/10861/719
dc.language.isoenen_US
dc.publisherЦентрална медицинска библиотека - МУ София / Central Medical Library - MU Sofiaen_US
dc.subjectarthrogryposis, epilepsy, cortical dysplasiaen_US
dc.titleArthrogryposis multiplex congenita, epileptic seizures and cortical dysplasia: a case reporten_US
dc.typeArticleen_US
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