Ad
related to: abnormal eeg with no seizures due to dementia diagnosis- Epilepsy Care
Options for Epilepsy Management.
Access a Free Treatment Guide.
- Generalized Seizures
Access a Free Treatment Guide.
Learn More About Seizures.
- Focal Seizures
Access a Free Treatment Guide.
Learn More About Seizures.
- Epilepsy Diagnosis
Neurological Diagnoses & Care.
Get the Free Epilepsy Guide.
- Epilepsy Care
Search results
Results from the WOW.Com Content Network
PNES episodes can be difficult to distinguish from epileptic seizures without the use of long-term video EEG monitoring.Some characteristics which may distinguish PNES from epileptic seizures include gradual onset, out-of-phase limb movement (in which left and right extremities jerk asynchronously or in opposite directions, as opposed to rhythmically and simultaneously as in epileptic seizures ...
Evidence for a diagnosis of epilepsy based on one or more of the following: Epileptiform abnormalities on electroencephalography (EEG). In a survey of all known cases, 43.6% have epileptiform abnormalities localised over the temporal or frontotemporal region on electroencephalography following the attack.
Congenital ophthalmic abnormalities; Childhood onset hyperkinetic movement disorder; Stereotypical motor behaviour; Moderate to profound developmental delay or intellectual disability; Sleep disturbance; Episodic agitation; Epileptic seizures are not a feature of this disorder (despite abnormal EEG) and head circumference is typically normal.
When used on its own, the term seizure usually refers to an epileptic seizure. The lay use of this word can also include sudden attacks of illness, loss of control, spasm or stroke. [ 4 ] Where the physician is uncertain as to the diagnosis, the medical term paroxysmal event and the lay terms spells , funny turns or attacks may be used.
Ohtahara syndrome (OS), also known as Early Infantile Developmental & Epileptic Encephalopathy (EIDEE) [2] is a progressive epileptic encephalopathy.The syndrome is outwardly characterized by tonic spasms and partial seizures within the first few months of life, [3] and receives its more elaborate name from the pattern of burst activity on an electroencephalogram (EEG).
Juvenile-onset DRPLA presents with ataxia and symptoms consistent with progressive myoclonus epilepsy [2] (myoclonus, multiple seizure types and dementia). Other symptoms that have been described include cervical dystonia , [ 3 ] corneal endothelial degeneration [ 4 ] autism , and surgery-resistant obstructive sleep apnea .
Amyloid-related imaging abnormalities (ARIA) are abnormal differences seen in magnetic resonance imaging of the brain in patients with Alzheimer's disease. ARIA is associated with anti-amyloid drugs, particularly human monoclonal antibodies such as aducanumab. [1] There are two types of ARIA: ARIA-E and ARIA-H.
The diagnosis may be made on the clinical features alone, along with tests to rule out other possible causes. An EEG will usually show the electrical features of epilepsy and slowing of brain activity in the affected hemisphere, and MRI brain scans will show gradual shrinkage of the affected hemisphere with signs of inflammation or scarring. [9]
Ad
related to: abnormal eeg with no seizures due to dementia diagnosis