Ads
related to: benign occipital epilepsy of childhood
Search results
Results From The WOW.Com Content Network
Pan. is also known as self-limiting focal epilepsy of childhood with occipital paroxysms and early-onset benign partial epilepsy with occipital paroxysms. There may be no known cause of this type of seizure, but these epilepsies may occur for a variety of reasons, such as brain tumors , infection, trauma and lesions , and idiopathic onset. [ 3 ]
Benign childhood occipital epilepsy, Panayiotopoulos type, Early-onset benign childhood occipital epilepsy Panayiotopoulos syndrome (named after C. P. Panayiotopoulos ) is a common idiopathic childhood-related seizure disorder that occurs exclusively in otherwise normal children (idiopathic epilepsy) and manifests mainly with autonomic ...
Idiopathic childhood occipital epilepsy of Gastaut (ICOE-G) is a pure but rare form of idiopathic occipital epilepsy that affects otherwise normal children and adolescents. [1] It is classified amongst benign idiopathic childhood focal epilepsies such as rolandic epilepsy and Panayiotopoulos syndrome .
Shvarts explains that many seizures are benign and won't require any or prolonged treatments. "But most seizures will need to be treated with anti-seizure medications," he says.
Benign occipital epilepsy of childhood (BOEC) is an idiopathic localization-related epilepsy and consists of an evolving group of syndromes. Most authorities include two subtypes, an early subtype with onset between three and five years, and a late onset between seven and 10 years.
Benign infantile epilepsy (BIE), also known as benign infantile seizures (BIS), is an epilepsy syndrome of which several forms have been described. The International League Against Epilepsy (ILAE) classify two main forms of the syndrome (familial and nonfamilial) [1] though several other forms have been described in the academic literature.
Ad
related to: benign occipital epilepsy of childhood