Results 81 to 90 of about 2,367 (191)

Proteus syndrome associated with hemimegalencephaly and Ohtahara syndrome: Report of two cases

, 2008
SummaryThe authors report two cases of Brazilian children with most of the common syndromic features of Proteus syndrome, such as asymmetric overgrowth of tissues, skin abnormalities, hypotonia and mental retardation.
Zandoná, Denise Isabel, Bragatti, José Augusto, Winckler, Maria Isabel Bragatti, Bastos, Halisson, Ohlweiler, Lygia, da Silva, Paula Fabiana Sobral, Mattos, Adriana, Riesgo, Rudimar Santos, de Albuquerque, Marco Antônio Veloso, Duarte, Rodrigo Dias   +9 more
core   +1 more source

Identification of a somatic mutation in the RHEB gene through high depth and ultra-high depth next generation sequencing in a patient with Hemimegalencephaly and drug resistant Epilepsy

, 2019
Malformations of cortical development are a frequent cause of drug-resistant Epilepsy and developmental delay. Hemimegalencephaly is a Malformation of cortical development characterized by enlargement of all or a part of one cerebral hemisphere. Germline
González Morón, Dolores, Novaro, Virginia, Silva, Walter, Chicco, Carla, García, María del Carmen, Perez Maturo, Josefina, Vega, Liliana Patricia, Ciraolo, Carlos, Christiansen, Silvia Beatriz, Consalvo, Damian, Kauffman, Marcelo Andres, Salinas Calderon, Valeria Macarena, Medina, Nancy, Perrone, Maria Cecilia, Piccirilli, María Victoria, Agosta, Guillermo   +15 more
core   +1 more source

Hemimegalencephaly: Seizure outcome in an infant after hemispherectomy [PDF]

, 2018
Isolated hemimegalencephaly (iHME) is a rare form of congenital malformation of cortical development characterized by enlargement of all or part of one cerebral hemisphere.
Abbas, Qalab, Chand, Prem, Manglani, Pooja   +2 more
core  

Postoperative EEG in Hemimegalencephaly [PDF]

European Neurology, 2012
Sheybani, Laurent, Korff, Christian, Maier, Oliver, Vargas Gomez, Maria Isabel, Schaller, Karl Lothard, Seeck, Margitta   +5 more
openaire   +4 more sources

Late Remission of Seizures After Functional Hemispherotomy in a Child With Congenital Middle Cerebral Artery Infarct

Archives of Epilepsy, 2017
Hemispherotomy can be a useful procedure in hemispheric syndromes, such as Rasmussen’s encephalitis, congenital stroke, or hemimegalencephaly. The seizures associated with these syndromes usually remit immediately after hemispherotomy.
Uğur IŞIK, Bahattin TANRIKULU, M. Memet ÖZEK   +2 more
doaj   +1 more source

Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

, 2013
Aims: Hemimegalencephaly (HME) is a rare malformation characterized by hamartomatous overgrowth limited to one cerebral hemisphere. HME may occur isolated or be associated with other syndromes.
Bürki, S, Staudt, M, Boltshauser, E, et al, Bosemani, T, Flores-Sarnat, L   +5 more
core   +1 more source

Hemimegalencephaly

Ultrasound Quarterly, 2011
Joseph, Reis, Gunvir, Gill, Susan, Voci, Jeevak, Almast   +3 more
  +5 more sources

Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders

Reproductive Biology and Endocrinology, 2003
A considerable number of central nervous system pathologies remain undiagnosed during the first two trimesters of pregnancy. This group of disorders includes anomalies of brain proliferation, migration and cortical organization.
Lev Dorit, Malinger Gustavo, Lerman-Sagie Tally   +2 more
doaj   +1 more source

Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia [PDF]

, 2015
Focal malformations of cortical development, including focal cortical dysplasia (FCD) and hemimegalencephaly (HME), are important causes of intractable childhood epilepsy.
Vinters, HV, Hossain, A, Mathern, GW, Couto, JA, Barkovich, AJ, Martin, B, Walsh, CA, Kwiatkowski, DJ, Poduri, A, Barry, BJ, Lacoursiere, CM, D'Gama, AM, Hatem, NE, Shendure, J, Boyle, EA, Geng, Y   +15 more
core   +1 more source

Reorganization of Sensorimotor Function after Functional Hemispherectomy Studied Using Near-Infrared Spectroscopy

, 2010
Hemimegalencephaly is a rare congenital disease that occurs with intractable epilepsy and is a childhood developmental disorder. A functional hemispherectomy is indicated for the treatment of hemimegalencephaly with intractable epilepsy.
Naoki Nakano, Yuji Higashimoto, Toshiki Matuoka, Yuko Sawada, Lin Suwen, Shohei Ohgi, Amami Kato, Noritsugu Honda, Kanji Fukuda   +8 more
core   +1 more source