Cargando…
Evolution of epilepsy in hemimegalencephaly from infancy to adulthood: Case report and review of the literature
Hemimegalencephaly (HME) is a rare disorder of cortical development with overgrowth of one cerebral hemisphere. Patients have intellectual delay, hemiparesis and severe epilepsy. Drug-resistant epilepsy is often treated with a hemispherectomy. We review the literature on HME natural history and repo...
Autores principales: | Ikeda, Kristin M., Mirsattari, Seyed M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5369267/ https://www.ncbi.nlm.nih.gov/pubmed/28377884 http://dx.doi.org/10.1016/j.ebcr.2017.02.002 |
Ejemplares similares
-
Hemimegalencephaly with polymicrogyria – a case report
por: RAUS, IULIAN, et al.
Publicado: (2016) -
Hemispherotomy in an infant with hemimegalencephaly
por: Kulkarni, Shilpa D., et al.
Publicado: (2015) -
Klippel-Trenaunay-Weber Syndrome with Hemimegalencephaly; Report of a Pediatric Case
por: Esmailzadeh, Hossein, et al.
Publicado: (2012) -
Infection-Induced Elevated Plasma Perampanel in a Patient with Hemimegalencephaly
por: Kinoshita, Yuya, et al.
Publicado: (2022) -
Ohtahara syndrome associated with hemimegalencephaly and intracranial lipoma
por: Gowda, Vykuntaraju K., et al.
Publicado: (2015)