Results 41 to 50 of about 844,102 (172)

Epilepsy and inborn errors of metabolism in adults: The diagnostic odyssey of a young woman with medium‐chain acyl‐coenzyme A dehydrogenase deficiency

Epilepsia Open, Volume 7, Issue 4, Page 810-816, December 2022., 2022
Abstract We describe a case of epileptic encephalopathy in a young woman with undiagnosed medium‐chain acyl‐coenzyme A dehydrogenase deficiency (MCADD), who presented with an early‐onset focal motor status epilepticus (SE) then followed by permanent left hemiplegia and drug‐resistant epilepsy with neurodevelopmental delay.
Ilaria Cani, Federica Pondrelli, Laura Licchetta, Raffaella Minardi, Tania Giangregorio, Barbara Mostacci, Lorenzo Muccioli, Lidia Di Vito, Anna Fetta, Carmen Barba, Carlo Alberto Castioni, Andrea Bordugo, Paolo Tinuper, Francesca Bisulli   +13 more
wiley   +1 more source

Dyke-Davidoff-Masson syndrome: A rare case report

Medical 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, Parth Singh Meena, Mahendra Jain, Krishan Kumar Sharma   +3 more
doaj   +1 more source

An unusual case of Dyke–Davidoff–Masson syndrome revealed by status epilepticus in a Malian patient

Clinical Case Reports, Volume 10, Issue 10, October 2022., 2022
Abstract The Duke–Davidoff–Masson syndrome (DDMS) is a rare neurological condition with unknown prevalence, globally. To date, <100 cases have been reported worldwide. We report the case of an 18‐year‐old patient admitted for status epilepticus seizure, and who presented a right hemiparesis, body asymmetry, joints ankylosis, and mental retardation ...
Samba O. Djimdé, Abdoulaye Yalcouyé, Abdou Koïta, Hassana Samir, Pofinet Kebkiba, Chrystelle Awovi Gueli, Alassane B. Maïga, Adama S. Sissoko, Guida Landouré   +8 more
wiley   +1 more source

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

Neurodevelopmental influences in psychosis: a case of left cerebral hemiatrophy and schizoaffective disorder

Psychiatry and Clinical Psychopharmacology, 2021
Cerebral hemiatrophy (or Dyke-Davidoff-Masson Syndrome) is a neurodevelopmental disorder characterized by atrophy or hypoplasia of one cerebral hemisphere accompanied by ipsilateral calvarial changes.
Asli Demirtas Tatlidede, Ayse Destina Yalcin, Tugba Guven Canpolat   +2 more
doaj   +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

Rasmussen encephalitis: Predisposing factors and their potential role in unilaterality

Epilepsia, Volume 63, Issue 1, Page 108-119, January 2022., 2022
Abstract Objective Rasmussen encephalitis (RE) is a progressive and destructive inflammatory disease of one hemisphere. Its cause is unknown. We investigated comorbidity and laterality factors that might predispose to RE. Methods We retrospectively compared the histories of 160 RE patients to those with genetic generalized epilepsy (n = 154) and those ...
Susanne Fauser, Christian E. Elger, Friedrich Woermann, Christian G. Bien   +3 more
wiley   +1 more source

Dyke–Davidoff–Masson syndrome with crossed cerebellar atrophy

South African Journal of Radiology, 2017
Dyke–Davidoff–Masson syndrome is a rare condition with classical, clinical and radiological changes – mental retardation, hemiparesis, facial asymmetry, seizures and cerebral hemiatrophy with calvarial changes.
Sanjay M. Khaladkar, Shishir Chauhan, Abhijit M. Patil, Siddappa G. Gandage, Surbhi Chauhan Kalra   +4 more
doaj   +1 more source

Dyke-Davidoff-Masson syndrome: A case report

Medical Journal of Dr. D.Y. Patil University, 2014
Dyke-Davidoff-Masson Syndrome (DDMS), also called as cerebral hemiatrophy, is a rare clinical condition characterized by seizures, facial asymmetry, contralateral spastic hemiplegia or hemiparesis, with learning difficulties.
Biswajyoti Rath, Maheswar Samant, Kali P Swain, Ashok K Mallick   +3 more
doaj   +1 more source