Results 11 to 20 of about 3,677 (133)

Dyke-Davidoff-Masson syndrome: Adult female patient with refractory epilepsy and global cognitive decline [PDF]

open access: yesBiomédica: revista del Instituto Nacional de Salud
The Dyke-Davidoff-Masson syndrome is characterized by the presence of cerebral hemiatrophy, craneal vault thickening, epileptic seizures, hemiparesis, and cognitive impairment. It is typically diagnosed in childhood and requires specific diagnostic tools
David Ríos   +2 more
doaj   +4 more sources

Dyke-Davidoff-Masson syndrome: A case report of an 11-year-old child managed for Erb's Palsy [PDF]

open access: yesRadiology Case Reports
Dyke-Davidoff-Masson syndrome (DDMS) is a rare neurological anomaly encompassing clinical features of seizures, contralateral hemiparesis, facial asymmetry, and intellectual dysfunction.
Abdullah Javed, MBBS, Dawood Javed, MBBS
doaj   +5 more sources

Dyke-Davidoff-Masson syndrome: a case report [PDF]

open access: yesBMC Neurology, 2018
Background Dyke-Davidoff-Masson syndrome is a rare condition of unknown frequency resulting from brain injury due to a multitude of causes; especially in early life.
Anna Misyail Abdul Rashid   +1 more
doaj   +3 more sources

An unusual case of Dyke–Davidoff–Masson syndrome revealed by status epilepticus in a Malian patient [PDF]

open access: yesClinical Case Reports (discontinued), 2022
Abstract The Duke–Davidoff–Masson syndrome (DDMS) is a rare neurological condition with unknown prevalence, globally. To date, <100 cases have been reported worldwide. We report the case of an 18‐year‐old patient admitted for status epilepticus seizure, and who presented a right hemiparesis, body asymmetry, joints ankylosis, and mental retardation ...
Abdoulaye Yalcouyé, Guida Landouré
exaly   +3 more sources

Dyke-Davidoff-Masson syndrome. [PDF]

open access: yesPan Afr Med J, 2021
We are presenting a case of 15-year-old male patient presented with weakness of right upper and lower limbs, difficulty lifting objects with the right hand. He was born full term to non-consanguineous parents with no significant antenatal or perinatal history.
Jain MJ, Kovela RK.
europepmc   +5 more sources

Dyke-Davidoff-Masson syndrome – A dainty spectrum with a diligent diagnosis [PDF]

open access: yesJournal of Family Medicine and Primary Care
Dyke-Davidoff-Masson syndrome is a rare condition of unknown frequency resulting from brain injury, especially in early life, due to a multitude of causes.
Anitha Palani   +4 more
doaj   +2 more sources

Adult Presentation of Dyke Davidoff Masson Syndrome With Schizoaffective Disorder — A Case Report

open access: yesKerala Journal of Psychiatry, 2018
Dyke Davidoff Masson syndrome (DDMS) is a rare disease with characteristic radiological features, seizures, mental retardation, facial asymmetry, and psychiatric manifestations. Here, we report a case of a 50-year-old female who had a refractory seizure
MK Dinesh Kumar, Denver Steven Pinto
doaj   +3 more sources

DYKE-DAVIDOFF-MASSON SYNDROME: MYOCLONIC SEIZURES AND HEMIHYPERTROPHY IN LATE CHILDHOOD: A CASE REPORT

open access: yesMalang Neurology Journal, 2022
Dyke-Davidoff-Masson Syndrome (DDMS) is a rare syndrome characterized with specific clinical and radiological findings due to involvement of the developing brain with cerebral hemiatrophy of one hemisphere.
Halil Ural Aksoy   +3 more
doaj   +3 more sources

Dyke-Davidoff-Masson syndrome

open access: yesIndian pediatrics, 2009
Dyke Davidoff Masson syndrome (DDMS) is characterized by seizures, facial asymmetry, contralateral hemiplegia and mental retardation. The characteristic radiologic features are cerebral hemiatrophy with homolateral hypertrophy of the skull and sinuses.
Mai-Lan Ho, Rohit Sharma, Mahmoud Rashed
core   +7 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   +2 more sources

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