Results 31 to 40 of about 438,209 (189)

CT of cerebral hemiatrophy [PDF]

American Journal of Roentgenology, 1980
Computed tomography (CT) findings in 10 cases of cerebral hemiatrophy are described. The CT appearance is typical and reflects the pathologic changes of unilateral loss of brain substance and calvarial thickening. In four patients with a mild form of the disease, a correct analysis of the pain skull radiographs was made only in retrospect. CT was found
openaire   +2 more sources

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

Case 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, Acharya A, Pokharel R, Rokaha PS, Rokaha PS, Luitel A.   +5 more
europepmc   +2 more sources

International League Against Epilepsy classification and definition of epilepsy syndromes with onset at a variable age: position statement by the ILAE Task Force on Nosology and Definitions

Epilepsia, Volume 63, Issue 6, Page 1443-1474, June 2022., 2022
Abstract The goal of this paper is to provide updated diagnostic criteria for the epilepsy syndromes that have a variable age of onset, based on expert consensus of the International League Against Epilepsy Nosology and Definitions Taskforce (2017–2021).
Kate Riney, Alicia Bogacz, Ernest Somerville, Edouard Hirsch, Rima Nabbout, Ingrid E. Scheffer, Sameer M. Zuberi, Taoufik Alsaadi, Satish Jain, Jacqueline French, Nicola Specchio, Eugen Trinka, Samuel Wiebe, Stéphane Auvin, Leonor Cabral‐Lim, Ansuya Naidoo, Emilio Perucca, Solomon L. Moshé, Elaine C. Wirrell, Paolo Tinuper   +19 more
wiley   +1 more source

Mendelian etiologies identified with whole exome sequencing in cerebral palsy

Annals of Clinical and Translational Neurology, Volume 9, Issue 2, Page 193-205, February 2022., 2022
Abstract Objectives Cerebral palsy (CP) is the most common childhood motor disability, yet its link to single‐gene disorders is under‐characterized. To explore the genetic landscape of CP, we conducted whole exome sequencing (WES) in a cohort of patients with CP.
Maya Chopra, Dustin L. Gable, Jamie Love‐Nichols, Alexa Tsao, Shira Rockowitz, Piotr Sliz, Elizabeth Barkoudah, Lucia Bastianelli, David Coulter, Emily Davidson, Claudio DeGusmao, David Fogelman, Kathleen Huth, Paige Marshall, Donna Nimec, Jessica Solomon Sanders, Benjamin J. Shore, Brian Snyder, Scellig S. D. Stone, Ana Ubeda, Colyn Watkins, Charles Berde, Jeffrey Bolton, Catherine Brownstein, Michael Costigan, Darius Ebrahimi‐Fakhari, Abbe Lai, Anne O'Donnell‐Luria, Alex R. Paciorkowski, Anna Pinto, John Pugh, Lance Rodan, Eugene Roe, Lindsay Swanson, Bo Zhang, Michael C. Kruer, Mustafa Sahin, Annapurna Poduri, Siddharth Srivastava   +38 more
wiley   +1 more source

Dyke-Davidoff-Masson syndrome: A case report with a literature review

Radiology Case Reports, 2022
Dyke-Davidoff-Masson syndrome (DDMS) is an uncommon neurological disease defined as cerebral hemiatrophy with a contralateral motor deficit, facial asymmetry, and seizures.
Mohamed Hamid, MD, Soukaina Cherradi, MD, Amal Satte, MD, Ahmed Bourazza, MD   +3 more
doaj   +1 more source

Dyke-Davidoff-Masson syndrome: Classical imaging findings

Journal of Pediatric Neurosciences, 2010
A 15-year-old female presented with seizures, right-sided hemiparesis, hemiatrophy of the right side of the body and mental retardation. MRI brain revealed characteristic features diagnostic of congenital type of cerebral hemiatrophy or Dyke-Davidoff ...
Paramdeep Singh, Kavita Saggar, Archana Ahluwalia   +2 more
doaj   +1 more source

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

Clin 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

A case of partial anomalous systemic venous drainage and perioperative detection of cerebral arteriovenous malformations

Annals of Pediatric Cardiology, 2021
We report a case of 8-year-old boy with unexplained desaturation and clubbing. Echocardiography showed anomalous drainage of right superior vena cava into left atrium. He did not have any neurological symptoms preoperatively.
Nilanjan Dutta, Debasis Das, Raghu Maruti Govindappa, Patralekha Das, Rangan Koley, Manish Kumar Sharma, Amitabha Chattopadhyay, Sanjiban Ghosh   +7 more
doaj   +1 more source

CEREBRAL HEMIATROPHY IN AN ADULT, WITH HEMIPLEGIA AND APHASIA [PDF]

American Journal of Psychiatry, 1901
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Harrington, A. H., Worcester, W. L.
openaire   +1 more source

Dyke Davidoff Masson Syndrome with Abdominal Epilepsy-Rare Presentation

Asian Journal of Medical Sciences, 2013
Dyke Davidoff Masson Syndrome (DDMS) with abdominal epilepsy, is a rare clinical condition. It is characterized by severe abdominal pain with seizures, facial asymmetry, contralateral hemiparesis, and mental retardation.
Shitanshu Srivastava
doaj   +1 more source