New on the MedlinePlus Epilepsy page:
National Institutes of Health
Epilepsy is a brain disorder that causes people to have recurring seizures. The seizures happen when clusters of nerve cells, or neurons, in the brain send out the wrong signals. People may have strange sensations and emotions or behave strangely. They may have violent muscle spasms or lose consciousness.
Epilepsy has many possible causes, including illness, brain injury, and abnormal brain development. In many cases, the cause is unknown.
Doctors use brain scans and other tests to diagnose epilepsy. It is important to start treatment right away. There is no cure for epilepsy, but medicines can control seizures for most people. When medicines are not working well, surgery or implanted devices such as vagus nerve stimulators may help. Special diets can help some children with epilepsy.
NIH: National Institute of Neurological Disorders and Stroke
- Computed Tomography (CT) -- Head (American College of Radiology, Radiological Society of North America)Also in Spanish
- EEG (Electroencephalogram) (Mayo Foundation for Medical Education and Research)
- Magnetic Resonance, Functional (fMRI) -- Brain(American College of Radiology, Radiological Society of North America) - PDFAlso in Spanish
- Pharmacogenetic Tests (National Library of Medicine)Also in Spanish
- Epilepsy Surgery (Mayo Foundation for Medical Education and Research)
- Seizure First Aid (Centers for Disease Control and Prevention)Also in Spanish
- Vagus Nerve Stimulation for Treating Epilepsy (American Academy of Neurology) - PDF
- Managing Epilepsy (Centers for Disease Control and Prevention)Also in Spanish
- Employees with Epilepsy/Seizure Disorder (Office of Disability Employment Policy)
- Sudden Unexpected Death in Epilepsy (SUDEP) (Centers for Disease Control and Prevention)
- Dravet Syndrome (National Institute of Neurological Disorders and Stroke)
- Lennox-Gastaut Syndrome (National Institute of Neurological Disorders and Stroke)
- Genetics Home Reference: Aicardi syndrome (National Library of Medicine)
- Genetics Home Reference: autosomal dominant nocturnal frontal lobe epilepsy (National Library of Medicine)
- Genetics Home Reference: autosomal dominant partial epilepsy with auditory features (National Library of Medicine)
- Genetics Home Reference: benign familial neonatal seizures (National Library of Medicine)
- Genetics Home Reference: beta-propeller protein-associated neurodegeneration (National Library of Medicine)
- Genetics Home Reference: CDKL5 deficiency disorder (National Library of Medicine)
- Genetics Home Reference: CHD2 myoclonic encephalopathy (National Library of Medicine)
- Genetics Home Reference: childhood absence epilepsy (National Library of Medicine)
- Genetics Home Reference: CLN4 disease (National Library of Medicine)
- Genetics Home Reference: CLN8 disease (National Library of Medicine)
- Genetics Home Reference: early infantile epileptic encephalopathy 1 (National Library of Medicine)
- Genetics Home Reference: epilepsy-aphasia spectrum (National Library of Medicine)
- Genetics Home Reference: FOXG1 syndrome (National Library of Medicine)
- Genetics Home Reference: GABA-transaminase deficiency (National Library of Medicine)
- Genetics Home Reference: genetic epilepsy with febrile seizures plus (National Library of Medicine)
- Genetics Home Reference: GM3 synthase deficiency (National Library of Medicine)
- Genetics Home Reference: guanidinoacetate methyltransferase deficiency (National Library of Medicine)
- Genetics Home Reference: hereditary hyperekplexia (National Library of Medicine)
- Genetics Home Reference: isodicentric chromosome 15 syndrome (National Library of Medicine)
- Genetics Home Reference: isolated lissencephaly sequence (National Library of Medicine)
- Genetics Home Reference: juvenile myoclonic epilepsy (National Library of Medicine)
- Genetics Home Reference: Koolen-de Vries syndrome (National Library of Medicine)
- Genetics Home Reference: Lafora progressive myoclonus epilepsy (National Library of Medicine)
- Genetics Home Reference: Lennox-Gastaut syndrome (National Library of Medicine)
- Genetics Home Reference: lipoid proteinosis (National Library of Medicine)
- Genetics Home Reference: lissencephaly with cerebellar hypoplasia (National Library of Medicine)
- Genetics Home Reference: malignant migrating partial seizures of infancy (National Library of Medicine)
- Genetics Home Reference: myoclonic epilepsy with ragged-red fibers (National Library of Medicine)
- Genetics Home Reference: PRICKLE1-related progressive myoclonus epilepsy with ataxia (National Library of Medicine)
- Genetics Home Reference: proximal 18q deletion syndrome (National Library of Medicine)
- Genetics Home Reference: pyridoxal 5'-phosphate-dependent epilepsy (National Library of Medicine)
- Genetics Home Reference: pyridoxine-dependent epilepsy (National Library of Medicine)
- Genetics Home Reference: ring chromosome 14 syndrome (National Library of Medicine)
- Genetics Home Reference: ring chromosome 20 syndrome (National Library of Medicine)
- Genetics Home Reference: SCN8A-related epilepsy with encephalopathy (National Library of Medicine)
- Genetics Home Reference: spinal muscular atrophy with progressive myoclonic epilepsy (National Library of Medicine)
- Genetics Home Reference: STXBP1 encephalopathy with epilepsy (National Library of Medicine)
- Genetics Home Reference: SYNGAP1-related intellectual disability (National Library of Medicine)
- Genetics Home Reference: Unverricht-Lundborg disease (National Library of Medicine)
- Craniotomy - slideshow (Medical Encyclopedia)Also in Spanish
- Curing the Epilepsies: The Promise of Research (National Institute of Neurological Disorders and Stroke)
- Epilepsy (National Institute of Neurological Disorders and Stroke)
- Targeting Epilepsy (Centers for Disease Control and Prevention) - PDF
- ClinicalTrials.gov: Epilepsy (National Institutes of Health)
- Article: A retrospective study of transcutaneous vagus nerve stimulation for poststroke...
- Article: Effects of CYP3A5 and UGT2B7 variants on steady-state carbamazepine concentrations...
- Article: Abnormal default-mode network homogeneity in patients with temporal lobe epilepsy.
- Epilepsy -- see more articles
- Find a Doctor (American Epilepsy Society)
- National Institute of Neurological Disorders and Stroke Also in Spanish
- Epilepsy (Nemours Foundation)Also in Spanish
- Infantile Spasms (National Institute of Neurological Disorders and Stroke)
- Epilepsy and Pregnancy (American Academy of Family Physicians)Also in Spanish
- Epilepsy and Pregnancy: What You Need to Know(Mayo Foundation for Medical Education and Research)
- Brain surgery (Medical Encyclopedia)Also in Spanish
- EEG (Medical Encyclopedia)Also in Spanish
- Epilepsy (Medical Encyclopedia)Also in Spanish
- Epilepsy - children (Medical Encyclopedia)Also in Spanish
- Epilepsy - children - discharge (Medical Encyclopedia)Also in Spanish
- Epilepsy or seizures - discharge (Medical Encyclopedia)Also in Spanish
No hay comentarios:
Publicar un comentario