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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. Jeavons syndrome - Wikipedia

    en.wikipedia.org/wiki/Jeavons_Syndrome

    Jeavons syndrome is a type of epilepsy. It is one of the most distinctive reflex syndromes of idiopathic generalized epilepsy characterized by the triad of eyelid myoclonia with and without absences, eye-closure-induced seizures, EEG paroxysms, or both, and photosensitivity. Eyelid myoclonia with or without absences is a form of epileptic ...

  4. Craniocervical instability - Wikipedia

    en.wikipedia.org/wiki/Craniocervical_instability

    Craniocervical instability (CCI) is a medical condition characterized by excessive movement of the vertebra at the atlanto-occipital joint and the atlanto-axial joint located between the skull and the top two vertebra, known as C1 and C2. [citation needed] The condition can cause neural injury and compression of nearby structures, including the ...

  5. Frontal lobe epilepsy - Wikipedia

    en.wikipedia.org/wiki/Frontal_lobe_epilepsy

    Frontal lobe epilepsy (FLE) is a neurological disorder that is characterized by brief, recurring seizures arising in the frontal lobes of the brain, that often occur during sleep. [1] It is the second most common type of epilepsy after temporal lobe epilepsy (TLE), and is related to the temporal form in that both forms are characterized by ...

  6. Panayiotopoulos syndrome - Wikipedia

    en.wikipedia.org/wiki/Panayiotopoulos_syndrome

    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 epileptic seizures and autonomic status epilepticus. [1] An expert consensus has defined Panayiotopoulos syndrome as ...

  7. Chiari malformation - Wikipedia

    en.wikipedia.org/wiki/Chiari_malformation

    1 in 100 (type I) [a] Named after. Hans Chiari. Julius Arnold. In neurology, the Chiari malformation (/ kiˈɑːri / kee-AR-ee; CM) is a structural defect in the cerebellum, characterized by a downward displacement of one or both cerebellar tonsils through the foramen magnum (the opening at the base of the skull).

  8. Occipital neuralgia - Wikipedia

    en.wikipedia.org/wiki/Occipital_neuralgia

    Occipital neuralgia. Occipital neuralgia (ON) is a painful condition affecting the posterior head in the distributions of the greater occipital nerve (GON), lesser occipital nerve (LON), third occipital nerve (TON), or a combination of the three. It is paroxysmal, lasting from seconds to minutes, and often consists of lancinating pain that ...

  9. Idiopathic childhood occipital epilepsy of Gastaut - Wikipedia

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

    The differential diagnosis of ICOE-G is mainly from symptomatic occipital epilepsy and migraine where misdiagnosis is high. The differential diagnosis from migraine should be easy because elementary visual hallucinations of occipital seizures develop rapidly within seconds, are brief in duration (2–3 minutes) are usually colored and circular.