Results 81 to 90 of about 1,407 (200)

Dyke Davidoff Masson Syndrome with Crossed Cerebellar Atrophy: A Case Report and Review of the Literature [PDF]

open access: yes, 2023
Dyke Davidoff Masson Syndrome (DDMS) is characterized clinically by hemiplegia or hemiparesis, mental retardation, and epilepsy and radiologically by cerebral hemiatrophy, ipsilateral calvarial thickening, and dilation and increased aeration of the ...
İzzet Ökçesiz   +2 more
core   +2 more sources

Acquired Dyke-Davidoff-Masson syndrome (DDMS)

open access: yesInternational Journal of Advanced Medical and Health Research, 2015
Dyke-Davidoff-Masson syndrome (DDMS) is characterized by cerebral hemiatrophy, contralateral hemiplegia, skull and facial asymmetries, seizures, and mental retardation. We present a case of acquired DDMS following meningoencephalitis.
Jitender Aneja   +3 more
doaj   +1 more source

Autoimmune‐associated seizure disorders

open access: yesEpileptic Disorders, Volume 26, Issue 4, Page 415-434, August 2024.
Abstract With the discovery of an expanding number of neural autoantibodies, autoimmune etiologies of seizures have been increasingly recognized. Clinical phenotypes have been identified in association with specific underlying antibodies, allowing an earlier diagnosis.
Kelsey M. Smith   +7 more
wiley   +1 more source

Progressive facial and cerebral hemiatrophy

open access: yesCleveland Clinic Journal of Medicine, 1984
A 43-year-old woman with progressive facial hemiatrophy had contralateral hemianopia and sensory loss. A computed-tomographic brain scan showed ipsilateral cerebral atrophy. The neurological and neuroradiological features of progressive facial hemiatrophy are reviewed.
openaire   +2 more sources

Dyke‐Davidoff‐Masson syndrome—A rare cause of recurrent seizures in adulthood

open access: yesClinical Case Reports, Volume 12, Issue 6, June 2024.
Key Clinical Message It is important to consider DDMS as a differential diagnosis in any patient with early childhood onset of epilepsy. Early diagnosis and optimal management are key to reducing the disabling effect of DDMS.
Patricia Afrim   +6 more
wiley   +1 more source

False localization of ictal activity by scalp EEG in candidates for hemispherectomy [PDF]

open access: yes, 1993
Two patients with intractable seizures and large structural lesions were candidates for hemispherectomy for seizure control. Repeated ictal EEGs recorded from scalp falsely localized seizure onset to the contralateral hemisphere. Intracarotid amobarbital
Baram, TZ, Mitchell, WG, Snead, OC
core   +1 more source

Two Cases of Dyke-Davidoff Masson Syndrome

open access: yesArchives of Epilepsy, 2017
Dyke-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 ...
Sabiha TEZCAN   +4 more
doaj   +1 more source

Presurgical evaluation and surgical treatment of medically refractory epilepsy [PDF]

open access: yes, 2018
Thanks to today's modern imaging examination techniques and especially to the common use of intracranial electrodes for localizing seizure foci, more and more patients with partial epilepsy can be treated microsurgically.
Siegel, Adrian
core  

Pyogenic Granuloma in a Patient of Sturge-Weber Syndrome with Bilateral Port Wine Stain- A Rare Case Report [PDF]

open access: yes, 2014
Sturge-Weber syndrome (SWS) also known as encephalotrigeminal angiomatosis. It is a neurocutaneous syndrome, characterized by a facial vascular birthmark and neurological abnormalities.
Mamata G. P   +3 more
core   +1 more source

Management of two cases of Rasmussen's Encephalitis at the department of pediatric neurology at the FANN National Hospital in Dakar, Senegal [PDF]

open access: yes, 2021
Rasmussen encephalitis is a rare autoimmune disease first described in the late 50s. It diagnosis requires multidisciplinary participation around the neuropediatrician.
DIOP SENE, Marième Soda   +5 more
core   +1 more source

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