Results 21 to 30 of about 239 (97)

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   +1 more source

Dyke-Davidoff-Masson Syndrome

open access: yesJournal of Nobel Medical College, 2012
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 ...
Naba Raj Koirala   +5 more
doaj   +3 more sources

Dyke⁃Davidoff⁃Masson syndrome: one case report

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2021
doi:10.3969/j.issn.1672⁃6731.2021.08 ...
HAO Jing⁃ru   +2 more
doaj   +1 more source

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   +1 more source

Cerebral hemiatrophy: Case series of three cases

open access: yesCHRISMED Journal of Health and Research, 2021
Pediatric cerebral hemiatrophy is a rare entity with widespread etiology. Imaging in form of computed tomography and magnetic resonance imaging is helpful in differentiating between the etiologies of hemiatrophy.
Suhail Rafiq   +3 more
doaj   +1 more source

Dyke-Davidoff-Masson syndrome: An endocrine perspective [PDF]

open access: yesRomanian Medical Journal, 2020
Dyke-Davidoff-Masson syndrome (DDMS) represents a severe disease that is caused by brain anomalies of different mechanisms early in life during fetal period or within first years after birth.
Cristina Dumitrescu   +8 more
doaj   +1 more source

Cutis Marmorata Telangiectatica Congenita Associated with Hemiatrophy

open access: yesCase Reports in Pediatrics, Volume 2020, Issue 1, 2020., 2020
Cutis marmorata telangiectatica congenita is characterized by the presence of a bluish‐purple reticulated cutaneous vascular network on the skin intermixed with telangiectasia and occasionally prominent veins at birth. Areas of the skin within the reticulated cutaneous vascular network may be normal, erythematous, atrophic, and, at times, ulcerated ...
Alexander K. C. Leung   +3 more
wiley   +1 more source

Dyke-Davidoff-Masson Syndrome: A Case Report

open access: yesInternational Journal of Medical Students, 2022
Background: Dyke-Davidoff-Masson syndrome (DDMS) is a neurological syndrome characterized by the presence of convulsions, facial asymmetry due to palsy of the facial nerve (CN VII), contralateral hemiplegia, and reduced intellectual capacity. The Case:
Gaurav M. Urs, Hitesh R. Doddabele
doaj   +1 more source

Dyke-Davidoff-Masson syndrome secondary to Sturge-Weber syndrome

open access: yesAsian Journal of Surgery
Zhiqin Lin   +3 more
doaj   +3 more sources

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