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Occipital epilepsy occurs equally in males and females and can occur at any age, although most patients’ onset begins in childhood. OE accounts for 5-10% of epilepsies, as it is a rare syndrome. Again, the age of onset varies based on the classification of OE a patient has.
Panayiotopoulos syndrome is now the formally approved nomenclature for this syndrome in the new International League against Epilepsy report on classification, [24] which abandoned a number of previously used descriptive terms such as early onset benign childhood epilepsy with occipital paroxysms, early onset benign childhood occipital epilepsy ...
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 .
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.
Benign Rolandic epilepsy or self-limited epilepsy with centrotemporal spikes (formerly benign childhood epilepsy with centrotemporal spikes (BECTS)) is the most common epilepsy syndrome in childhood. [ 1 ] [ 2 ] Most children will outgrow the syndrome (it starts around the age of 3–13 with a peak around 8–9 years and stops around age 14 ...
Benign familial infantile epilepsy (BFIE) is an epilepsy syndrome. [1] Affected children, who have no other health or developmental problems, develop seizures during infancy. These seizures have focal origin within the brain but may then spread to become generalised seizures. The seizures may occur several times a day, often grouped in clusters ...
In 1957 he described the hemiconvulsion-hemiplegia-epilepsy(HHE) syndrome, [5] in 1961 [6] and 1966 [7] the Lennox-Gastaut syndrome, and in 1981 [8] and 1982 [9] the late variant of the benign childhood epilepsy with occipital paroxysms. After the Second World War he was influential in reactivating the International League Against Epilepsy ...