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Two Cases of Dyke-Davidoff Masson Syndrome

dc.contributor.authorULUKAN, Çağrı
dc.contributor.authorAydin, Nursel
dc.contributor.authorERDOĞAN, SEYDA
dc.contributor.authorPEKER, ELİF
dc.contributor.authorTezcan, Sabiha
dc.date.accessioned2022-02-18T09:30:01Z
dc.date.available2022-02-18T09:30:01Z
dc.date.issued2017
dc.identifier.citationTezcan S., ULUKAN Ç., ERDOĞAN S., PEKER E., Aydin N., "Two Cases of Dyke-Davidoff Masson Syndrome", EPILEPSI, cilt.23, sa.3, ss.131-134, 2017
dc.identifier.othervv_1032021
dc.identifier.otherav_419fe341-761f-4c0f-99cb-e14d14bed2b7
dc.identifier.urihttp://hdl.handle.net/20.500.12627/177341
dc.identifier.urihttps://doi.org/10.14744/epilepsi.2017.03016
dc.description.abstractDyke-Davidoff Masson Syndrome (DDMS) is a rare syndrome characterized by seizures, facial asymmetry, and contralateral hemiplegia or hemiparesis. The typical radiological features of DDMS include cerebral hemiatrophy with ipsilateral hypertrophy of the skull and sinuses. It is usually diagnosed in childhood. Presently described are 2 rare cases of DDMS that were diagnosed in adults based on magnetic resonance imaging of the brain.
dc.language.isoeng
dc.subjectNeurology
dc.subjectNeurology (clinical)
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleTwo Cases of Dyke-Davidoff Masson Syndrome
dc.typeMakale
dc.relation.journalEPILEPSI
dc.contributor.departmentAnkara Üniversitesi , ,
dc.identifier.volume23
dc.identifier.issue3
dc.identifier.startpage131
dc.identifier.endpage134
dc.contributor.firstauthorID3385117


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