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  2. Occipital epilepsy - Wikipedia

    en.wikipedia.org/wiki/Occipital_epilepsy

    Seizures originate in the occipital lobe and account for 5 to 10 percent of all epileptic seizure types. Generally, this type of epilepsy can have an onset anywhere from 1–17 years old in children, but the patient prognosis is good. Since the event is located in the occipital lobe, symptoms may occur spontaneously and include visual stimuli.

  3. Panayiotopoulos syndrome - Wikipedia

    en.wikipedia.org/wiki/Panayiotopoulos_syndrome

    The same child may have brief or prolonged seizures and autonomic manifestations may be severe or inconspicuous. The full emetic triad (nausea, retching, vomiting) culminates in vomiting in 74% of the seizures; in others only nausea or retching occur, and in a few, none of the emetic symptoms are apparent. [citation needed]

  4. Epilepsy in children - Wikipedia

    en.wikipedia.org/wiki/Epilepsy_in_children

    Epilepsy is more common among children than adults, affecting about 6 out of 1000 US children that are between the age of 0 to 5 years old. [2] The epileptic seizures can be of different types depending on the part of the brain that was affected, seizures are classified in 2 main types partial seizure or generalized seizure .

  5. Salt and pepper syndrome - Wikipedia

    en.wikipedia.org/wiki/Salt_and_pepper_syndrome

    The first features of the syndrome start off with feeding difficulties, constant irritability, frequent vomiting, and hypotonia. [11] [6] [10] The second manifestations of this condition are frequent seizures whose type can vary between patients, but usually consist of tonic-clonic seizures. These usually start sometime during the baby's first ...

  6. Idiopathic childhood occipital epilepsy of Gastaut - Wikipedia

    en.wikipedia.org/wiki/Idiopathic_childhood...

    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 .

  7. Epilepsy syndromes - Wikipedia

    en.wikipedia.org/wiki/Epilepsy_syndromes

    Syndromes are characterized into 4 groups based on epilepsy type: [1] a. Generalized onset epilepsy syndromes. These epilepsy syndromes have only generalized-onset seizures and include both the idiopathic generalized epilepsies (specifically childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy and epilepsy with generalized tonic- clonic seizures alone), as well as ...

  8. Abdominal epilepsy - Wikipedia

    en.wikipedia.org/wiki/Abdominal_epilepsy

    Abdominal epilepsy is marked by GI symptoms such as abdominal pain followed by uncontrollable vomiting, usually preceded by lethargy. Lethargy and confusion is the most common neurological symptoms associated with abdominal epilepsy. Other symptoms include generalized tonic-clonic seizures followed by sleep, and unresponsiveness.

  9. Causes of seizures - Wikipedia

    en.wikipedia.org/wiki/Causes_of_seizures

    Approximately 40% of children who experience a febrile seizure will have another one. [26] In those with epilepsy, fever can trigger a seizure. Additionally, in some, gastroenteritis, which causes vomiting and diarrhea, can lead to diminished absorption of anticonvulsants, thereby reducing protection against seizures. [27]