Results 11 to 20 of about 1,463 (166)

Case Report of Rasmussen's Encephalitis With a Decade of Refractory Epilepsy and Hemispheric Atrophy. [PDF]

open access: yesClin Case Rep
ABSTRACT Rasmussen's encephalitis (RE) is a rare, chronic inflammatory neurological disorder affecting one cerebral hemisphere and presenting with drug‐resistant epilepsy, progressive hemiparesis, and cognitive decline. This case report describes the clinical course and management of a 21‐year‐old patient with refractory epilepsy and progressive ...
Al-Badri S   +7 more
europepmc   +2 more sources

High-Frequency Ultrasound Assessment of Skin Thickness Following Lipofilling in Facial Sclerosing Dermatoses: A Case Series. [PDF]

open access: yesJ Cosmet Dermatol
Journal of Cosmetic Dermatology, Volume 24, Issue 5, May 2025.
Gomez-Martinez S   +12 more
europepmc   +2 more sources

Phenotypic Spectrum and Diagnostic Challenges in Klippel-Trenaunay Syndrome: A Case Series. [PDF]

open access: yesClin Case Rep
ABSTRACT Klippel‐Trénaunay syndrome (KTS) is a rare congenital disorder characterized by the triad of capillary malformations, venous varicosities, and soft tissue or bony hypertrophy. This case series highlights rare and atypical presentations of KTS, emphasizing the importance of a multidisciplinary diagnostic approach.
Hameed M, Ali T, Haque MA.
europepmc   +2 more sources

Adult Presentation of Dyke-Davidoff-Masson Syndrome, a Radiological Enigma: A Case Report. [PDF]

open access: yesCase Rep Radiol
Introduction and Importance: Dyke–Davidoff–Masson syndrome (DDMS) is a rare neurological condition characterized by focal or generalized drug‐resistant epilepsy, hemiparesis, face or body asymmetry with atrophy, and cognitive impairment in early childhood and adulthood. DDMS is generally diagnosed in the paediatric age group.
Paudel S   +5 more
europepmc   +2 more sources

Porencephalic cyst with ipsilateral cerebral hemiatrophy presenting with generalized tonic–clonic seizures and neuropsychiatric features: A case report with literature review

open access: yesArchives of Mental Health, 2023
Porencephalic cysts in combination with cerebral hemiatrophy have been described rarely. Herewith, we describe an 18-year-old female who presented with seizures, neuropsychiatric symptoms, and mild intellectual disability without facial asymmetry or ...
Bhogaraju Anand   +2 more
doaj   +1 more source

Dyke-Davidoff-Masson syndrome: A study of clinicoradiological variability in hemiplegia, hemiatrophy and epilepsy patients

open access: yesCHRISMED Journal of Health and Research, 2014
Context: Clinicoradiological variability expansion in Dyke-Davidoff-Masson syndrome (DDMS) or hemiplegia, hemiatrophy and epilepsy (HHE) patients. Aims: To explore clinicoradiological features, associated abnormalities and refractoriness issues to ...
Amita Bhargava   +5 more
doaj   +1 more source

Subcortical and brainstem hemiatrophy accompanied by iron deposition in a patient with hemiparkinsonism-hemiatrophy syndrome: a case report

open access: yesBMC Neurology, 2021
Background There is no established pathogenesis of hemiparkinsonism-hemiatrophy syndrome (HPHA), and the varied clinical presentations have been reported in several case studies.
Su Jin Chung
doaj   +1 more source

Dyke-Davidoff-Masson syndrome: A rare case report

open access: yesMedical Journal of Dr. D.Y. Patil University, 2016
Dyke-Davidoff-Masson syndrome (DDMS) is a rare clinical condition characterized by seizures, facial asymmetry, contralateral spastic hemiplegia or hemiparesis, with learning difficulties. It is also called as cerebral hemiatrophy.
Charan Singh Jilowa   +3 more
doaj   +1 more source

FACIAL HEMIATROPHY [PDF]

open access: yesThe Journal of Nervous and Mental Disease, 1911
n ...
openaire   +2 more sources

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