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Fetal electroencephalography, also known as prenatal EEG includes any recording of electrical fluctuations arising from the brain of a fetus. Doctors and scientists use EEGs to detect and characterize brain activity, such as sleep states, potential seizures, or levels of a coma .
Although children with benign infantile epilepsy typically have a normal EEG between seizures, some infants have been found to have a characteristic abnormal EEG during sleep. Called benign infantile focal epilepsy with midline spikes and waves during sleep, these infants have few seizures and there may often be a family history. [4]
It can be caused by a number of different reasons, some benign, unknown reasons, but also are commonly associated with lesions, tumors, and encephalopathies. [3] ...
He had been seizing consecutively for the first 30 minutes of the EEG.” “He was likely having one consecutive seizure for this entire first week of life,” she shares. “After 30 minutes ...
EEG can detect abnormal electrical discharges such as sharp waves, spikes, or spike-and-wave complexes, as observable in people with epilepsy; thus, it is often used to inform medical diagnosis. EEG can detect the onset and spatio-temporal (location and time) evolution of seizures and the presence of status epilepticus.
It is an abnormal interictal pattern, consisting of high amplitude and irregular waves and spikes in a background of chaotic and disorganized activity seen on electroencephalogram (EEG), and frequently encountered in infants diagnosed with infantile spasms, although it can be found in other conditions such as tuberous sclerosis.
Hormones and pregnancy issues. Hormonal changes and pregnancy can shift seizure activity and the use of antiepileptic drugs can alter the efficacy of hormones as well as cause congenital malformations in fetuses. [24] Seizure control in pregnant women is very important to the welfare of both the developing fetus and the mother.
Ohtahara syndrome (OS), also known as Early Infantile Developmental & Epileptic Encephalopathy (EIDEE) [2] is a progressive epileptic encephalopathy.The syndrome is outwardly characterized by tonic spasms and partial seizures within the first few months of life, [3] and receives its more elaborate name from the pattern of burst activity on an electroencephalogram (EEG).