Dyke-Davidoff-Masson syndrome: A rare case of hemiatrophy of brain—Case report from Nepal
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
Dyke-Davidoff-Masson Syndrome a Rare Cause of Cerebral Hemiatrophy: A Case Report
Cerebral hemiatrophy or Dyke-Davidoff-Masson syndrome (DDMS) is a rare clinical and radiological entity, characterized by seizures, facial asymmetry, contralateral hemiplegia or hemiparesis and mental retardation. These findings are due to a brain lesion
C. Chbichib +5 more
semanticscholar +1 more source
Cerebral hemiatrophy associated with Chronic Subdural Hematoma- Rare Cadaveric Observations
Cerebral hemiatrophy is an infrequent neuroimaging observation of varied etiologies, classified into two wide categories: congenital and acquired. Chronic subdural hematoma is hypothesised to be associated with the aetiology of brain atrophy.
Kumar Sambhav +4 more
semanticscholar +1 more source
Adult Presentation of Dyke-Davidoff-Masson Syndrome, a Radiological Enigma: A Case Report. [PDF]
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
Dyke-Davidoff-Masson Syndrome (DDMS) in Adult: A Rare Case in Rural Area
Highlight: • Dyke-Davidoff-Masson syndrome (DDMS) is an uncommon neurological disease defined as cerebral hemiatrophy with a contralateral motor deficit, facial asymmetry, and seizures.
Indra Pramanasari
doaj +1 more source
Phenotypic Spectrum and Diagnostic Challenges in Klippel-Trenaunay Syndrome: A Case Series. [PDF]
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
Abstract This study evaluated sleep and respiratory abnormalities, and their relationship with seizures, in adults with developmental and epileptic encephalopathies (DEEs). We studied consecutive adults with DEEs undergoing inpatient video‐EEG monitoring and concurrent polysomnography between December 2011 and July 2022.
Shobi Sivathamboo +7 more
wiley +1 more source
Dyke–Davidoff–Masson syndrome presenting as recurrent chronic headache in the late adult life
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
Hemiatrophy of The Cerebral Hemisphere with Contralateral Cerebellar Atrophy: A Case Report
Childhood cerebral hemiatrophy is a rare clinical condition. Its causes are numerous, but they can be divided into two categories: congenital and acquired.
Prakash Dhakal +2 more
semanticscholar +1 more source
Clinical and radiological description of 120 pediatric stroke‐like episodes
Abstract Background and purpose Stroke‐like episodes (SLEs) are defined as acute onset of neurological symptoms mimicking a stroke and radiological lesions non‐congruent to vascular territory. We aimed to analyze the acute clinical and radiological features of SLEs to determine their pathophysiology.
Chloe Durrleman +11 more
wiley +1 more source

