Dyke-Davidoff-Masson Syndrome: A Classic Case Report.

Autor:	Dhawan S; Radiodiagnosis, NKP Salve Institute of Medical Sciences and Research Centre, Nagpur, IND., Rathod NR; Radiodiagnosis, NKP Salve Institute of Medical Sciences and Research Centre, Nagpur, IND., Dhok A; Radiodiagnosis, NKP Salve Institute of Medical Sciences and Research Centre, Nagpur, IND., Mitra K; Radiodiagnosis, NKP Salve Institute of Medical Sciences and Research Centre, Nagpur, IND., Chordiya R; Radiodiagnosis, NKP Salve Institute of Medical Sciences and Research Centre, Nagpur, IND.
Jazyk:	angličtina
Zdroj:	Cureus [Cureus] 2023 Feb 02; Vol. 15 (2), pp. e34570. Date of Electronic Publication: 2023 Feb 02 (Print Publication: 2023).
DOI:	10.7759/cureus.34570
Abstrakt:	Dyke-Davidoff-Masson syndrome (DDMS) is a rare neurological disorder found in children as well as adults. It is characterized by hemi cerebral atrophy. To date, very few cases of this disorder have been reported. Radiological imaging including magnetic resonance imaging (MRI) and computed tomography (CT) are accurate tools for the diagnosis of DDMS. We present a case of a 13-year-old female child who came with complaints of multiple episodes of generalized tonic-clonic seizures. In our case, clinical history and imaging with CT and MRI were accurate enough to diagnose DDMS. Competing Interests: The authors have declared that no competing interests exist. (Copyright © 2023, Dhawan et al.)
Databáze:	MEDLINE
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