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

  • 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

    Vascular dementia (VaD) is a general term describing problems with reasoning, planning, judgment, memory, and other thought processes caused by brain damage from impaired blood flow to the brain. Cognitive rehabilitation and physical therapy are the mainstays of dementia treatment, although often ineffective[…][ncbi.nlm.nih.gov]

  • 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 the most common inherited form of cognitive deficiency in humans and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion, inactivating the X-linked FMR1 gene, leads to the absence of the fragile X mental retardation protein. FMRP is a selective RNA-binding[…][ncbi.nlm.nih.gov]

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