Search results
Results from the WOW.Com Content Network
Epilepsy-intellectual disability in females also known as PCDH19 gene-related epilepsy or epileptic encephalopathy, early infantile, 9 (EIEE9), is a rare type of epilepsy that affects predominantly females and is characterized by clusters of brief seizures, which start in infancy or early childhood, and is occasionally accompanied by varying degrees of cognitive impairment.
An expert consensus has defined Panayiotopoulos syndrome as "a benign age-related focal seizure disorder occurring in early and mid-childhood. It is characterized by seizures, often prolonged, with predominantly autonomic symptoms, and by an EEG [electroencephalogram] that shows shifting and/or multiple foci, often with occipital predominance." [2]
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).
This is an accepted version of this page This is the latest accepted revision, reviewed on 17 February 2025. The following is a list of mental disorders as defined at any point by the Diagnostic and Statistical Manual of Mental Disorders (DSM) or the International Classification of Diseases (ICD). A mental disorder, also known as a mental illness, mental health condition, or psychiatric ...
The production of seizure-like symptoms is not under voluntary control; [10] [11] symptoms which are feigned or faked voluntarily would fall under the categories of factitious disorder or malingering. [12] Risk factors for PNES include having a history of head injury, and having a diagnosis of epilepsy. [13]
Non-epileptic seizures – these may look like epileptic seizures or faints; Movement disorders including tremors, dystonia (spasms), myoclonus (jerky movements) Visual symptoms including loss of vision or double vision; Speech symptoms including dysphonia (whispering speech), slurred or stuttering speech
From 2018 through mid-2022, visits among people younger than 17 jumped 107.4% across all eating disorders. (Trilliant Health)
Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy (SMEI), is an autosomal dominant genetic disorder which causes a catastrophic form of epilepsy, with prolonged seizures that are often triggered by hot temperatures or fever. [1]