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10 Possible Causes for Paroxysmal Activity - Sharp-Waves Temporal

  • Epilepsy

    OBJECTIVE: To study seizure control and rates of foetal malformation in pregnancies of women with epilepsy treated with antiepileptic drug polytherapy. METHODS: The use of conventional statistical methods to analyse the Australian Pregnancy Register records of 1810 pregnancies in women with epilepsy, 508 treated[…][ncbi.nlm.nih.gov]

  • Vascular Dementia

    To view the fulltext, please log in To view the pdf, please log in Buy FullText & PDF Unlimited re-access via MyKarger Unrestricted printing, no saving restrictions for personal use read more CHF 38.00 * EUR 35.00 * USD 39.00 * Select KAB Buy a Karger Article Bundle (KAB) and profit from a discount ! If you would[…][dx.doi.org]

  • Encephalitis

    Encephalitis is inflammation of the brain. Severity is variable. Symptoms may include headache, fever, confusion, a stiff neck, and vomiting. Complications may include seizures, hallucinations, trouble speaking, memory problems, and problems with hearing.Causes of encephalitis include viruses such as herpes simplex virus[…][en.wikipedia.org]

  • Rolandic Epilepsy

    Benign Rolandic epilepsy or benign childhood epilepsy with centrotemporal spikes (BCECTS) is the most common epilepsy syndrome in childhood. Most children will outgrow the syndrome (it starts around the age of 3–13 with a peak around 8–9 years and stops around age 14–18), hence the label benign. The seizures,[…][en.wikipedia.org]

  • Creutzfeldt Jakob Disease

    Prion diseases are unique transmissible neurodegenerative diseases that have diverse phenotypes and can be familial, sporadic, or acquired by infection. Recent findings indicate that the PrP genotype and the PrP(Sc) type have a major influence on the disease phenotype in both sporadic and familial human prion[…][ncbi.nlm.nih.gov]

  • Periventricular Leukomalacia

    2015 ICD-9-CM Diagnosis Code 779.7 Periventricular leukomalacia 2015 Billable Thru Sept 30/2015 Non-Billable On/After Oct 1/2015 ICD-9-CM 779.7 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 779.7 should only be used for claims with a date of service on or before[…][icd9data.com]

  • Fragile X Syndrome

    Fragile X syndrome is a genetic condition caused by a mutation of the fragile X mental retardation 1 (FMR1) gene on the X chromosome. Fragile X syndrome in males is usually more severe than in females and males are never asymptomatic. This is because males have only one X chromosome (unlike females that have 2[…][symptoma.com]

  • Metabolic Encephalopathy

    ., frontal intermittent rhythmic delta activity (FIRDA), or spikes and sharp waves as well as spike-wave discharges in temporal regions. [37] In hyponatremia, EEG detects[neurologyindia.com] […] diffuse slowing in the theta range, followed by paroxysmal delta activity and FIRDA or periodic delta waves, as well as the occurrence of periodic lateralized epileptiform[neurologyindia.com]

  • Uremic Encephalopathy

    ., frontal intermittent rhythmic delta activity (FIRDA), or spikes and sharp waves as well as spike-wave discharges in temporal regions. [37] In hyponatremia, EEG detects[neurologyindia.com] […] diffuse slowing in the theta range, followed by paroxysmal delta activity and FIRDA or periodic delta waves, as well as the occurrence of periodic lateralized epileptiform[neurologyindia.com]

  • Toxic Encephalopathy

    ., frontal intermittent rhythmic delta activity (FIRDA), or spikes and sharp waves as well as spike-wave discharges in temporal regions. [37] In hyponatremia, EEG detects[neurologyindia.com] […] diffuse slowing in the theta range, followed by paroxysmal delta activity and FIRDA or periodic delta waves, as well as the occurrence of periodic lateralized epileptiform[neurologyindia.com]

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