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  2. CDKL5 deficiency disorder - Wikipedia

    en.wikipedia.org/wiki/CDKL5_deficiency_disorder

    Note: many adolescents and young adults may have CDD but were never tested since such tests were not available when they were infants. Therefore, epilepsy panels for CDD and other genes should be considered in such individuals. [8] A diagnostic ICD-10 code has been assigned to CDKL5 deficiency disorder: G40.42 (since 2020). [9]

  3. Psychogenic non-epileptic seizure - Wikipedia

    en.wikipedia.org/wiki/Psychogenic_non-epileptic...

    Risk factors for PNES include having a history of head injury, and having a diagnosis of epilepsy. [13] Approximately 10–30% of people diagnosed with PNES also have an epilepsy diagnosis. People diagnosed with PNES commonly report physical, sexual, or emotional trauma. [14] [15] [16]

  4. SYNGAP1-related intellectual disability - Wikipedia

    en.wikipedia.org/wiki/SYNGAP1-related...

    F78.A1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2023 edition of ICD-10-CM F78.A1 became effective on October 1, 2022. This is the American ICD-10-CM version of F78.A1 - other international versions of ICD-10 F78.A1 may differ.

  5. Category:Epilepsy - Wikipedia

    en.wikipedia.org/wiki/Category:Epilepsy

    Generally, diseases outlined within the ICD-10 codes G40 within Chapter VI: Diseases of the nervous system should be included in this category. Articles related to the neurological disorder epilepsy .

  6. Non-epileptic seizure - Wikipedia

    en.wikipedia.org/wiki/Non-epileptic_seizure

    Non-epileptic seizures (NES), also known as pseudoseizures, non-epileptic attack disorder (NEAD), functional seizures, or dissociative seizures, are paroxysmal events that appear similar to an epileptic seizure, but do not involve abnormal, rhythmic discharges of neurons in the brain. [1]

  7. Dravet syndrome - Wikipedia

    en.wikipedia.org/wiki/Dravet_syndrome

    The International Dravet Syndrome Epilepsy Action League (IDEA League) conducted a study in which they concluded that 31 of 833 DS patients died within 10 years. The average death age was 4.6 years, with 19 of 31 deaths because of SUDEP, 10 from status epilepticus, 1 from ketoacidosis, and 1 from an accident. It is unclear what duration ...

  8. Lennox–Gastaut syndrome - Wikipedia

    en.wikipedia.org/wiki/Lennox–Gastaut_syndrome

    Lennox–Gastaut syndrome (LGS) is a complex, rare, and severe childhood-onset epilepsy syndrome. It is characterized by multiple and concurrent seizure types including tonic seizure, cognitive dysfunction, and slow spike waves on electroencephalogram (EEG), which are very abnormal. [1]

  9. Seizure - Wikipedia

    en.wikipedia.org/wiki/Seizure

    Strokes, brain bleeds, and traumatic brain injury can all also lead to epilepsy if seizures re-occur. If the first seizure occurs more than 7 days following a stroke, there is a higher chance of the person developing epilepsy. [27] Post-stroke epilepsy accounts for 30%-50% of new epilepsy cases. [27]