Create issue ticket

7 Possible Causes for Paroxysmal Activity - Sharp-Waves Frontal Bilaterally

  • Epilepsy

    Epilepsy is a brain disorder in which a person has repeated seizures over time. Seizures are episodes of uncontrolled and abnormal firing of brain cells that may cause changes in attention or behavior. Epilepsy occurs when changes in the brain cause it to be too excitable or irritable. As a result, the brain sends[…][medlineplus.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

    Rolandic epilepsy, sometimes also referred to as benign childhood epilepsy with centrotemporal spikes, is the most common type of childhood epilepsy. Spontaneous remission before puberty is observed in the majority of cases. Characteristic RE seizures are hemifacial motor seizures, sometimes also motorsensory[…][symptoma.com]

  • 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]

Further symptoms