Results 21 to 30 of about 1,837 (197)

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

Dyke-Davidoff-Masson syndrome: A rare case of hemiatrophy of brain—Case report from Nepal

open access: yesRadiology Case Reports, 2022
Dyke-Davidoff-Masson syndrome (DDMS) is a rare neurological disorder that results from brain injury during intrauterine or early years of life. Prominent cortical sulci, dilated lateral ventricles, cerebral hemiatrophy, hyperpneumatization of the sinus ...
Prakash Dhakal, MD   +4 more
doaj   +1 more source

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

Progressive Facial Hemiatrophy Revisited [PDF]

open access: yes, 2011
ObjectiveTo report a case of progressive facial hemiatrophy with unusual features of contralateral brain atrophy and transcranial Doppler ultrasound evidence of autonomic dysfunction.DesignCase report.SettingA teaching hospital.PatientA 63-year-old man ...
Hong-Liang Zhang   +5 more
core   +1 more source

Dyke–Davidoff–Masson syndrome presenting as recurrent chronic headache in the late adult life

open access: yesBrain Circulation, 2020
Dyke–Davidoff–Masson syndrome (DDMS) (also referred to as cerebral hemiatrophy) is a rare condition characterized by seizures, facial asymmetry, contralateral spastic hemiplegia, or hemiparesis, with or without learning difficulties.
Wafa Ali Aldhaleei   +2 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 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

Homonymous hemiatrophy of ganglion cell layer from retrochiasmal lesions in the visual pathway. [PDF]

open access: yes, 2020
OBJECTIVE To determine the temporal evolution, morphology, and frequency of macular ganglion cell atrophy in patients with retrochiasmal lesions of the visual pathway. METHODS In a consecutive retrospective case series, we identified 47 patients
Mühlemann, Fabian   +6 more
core   +1 more source

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