What EARLY INFANTILE EPILEPTIC ENCEPHALOPATHY means: Early Infantile Epileptic Encephalopathy - or Ohtahara syndrome is a neurological disorder characterized by seizures. The disorder affects newborns, usually within the first three months of life (most often within the first 10 days) in the form of epileptic seizures. Infants have primarily tonic seizures, but may also experience partial seizures, and rarely, myoclonic seizures. Most infants with the disorder show significant underdevelopment of part or all of the cerebral hemispheres.
- Definition Erb-Duchenne And Dejerine-Klumpke Palsies:
- Dictionary Dejerine-Klumpke Palsies - The brachial plexus is a network of nerves that conducts signals from the spine to the shoulder, arm, and hand. Brachial plexus injuries are caused by damage to those early infantile epileptic encephalopathy.
- Definition Encephaloceles:
- Dictionary are rare neural tube defects characterized by sac-like protrusions of the brain and the membranes that cover it through openings in the skull. These defects are caused by failure of the neural tube early infantile epileptic encephalopathy.
- Definition Encephalotrigeminal Angiomatosis:
- Dictionary Encephalotrigeminal Angiomatosis - A rare genetic disorder characterized by excessive blood vessel growth, calcium accumulation inside the brain and seizures early infantile epileptic encephalopathy.
- Definition Extrapontine Myelinolysis:
- Dictionary Myelinolysis - (CPM) is a neurological disorder that most frequently occurs after too rapid medical correction of sodium deficiency (hyponatremia). The rapid rise in sodium concentration is early infantile epileptic encephalopathy.