Ohtahara syndrome

Ohtahara Syndrome (OS) is the earliest-developing age-related epileptic encephalopathy. It is an extremely debilitating progressive neurological disorder, involving intractable seizures and severe mental retardation. No single cause has been identified, although in many cases structural brain damage is present.^[1] The syndrome is outwardly characterized by tonic spasms and partial seizures, and receives its more elaborate name from the pattern of burst activity in an EEG.

There is severe atrophy of both hemispheres of the brain.

No single cause of OS has been identified. Less often, the root of the disorder is an underlying metabolic syndrome. No genetic connection has been established.^[2]

Seizure onset within the first three months (and often first 10 days) of life.

• Mental retardation
• Infections

Infants with Ohtahara syndrome make very little developmental progress. They remain totally dependent on others and often feed poorly. They often die within the first two years of life because of repeated chest infections. Those who do survive will be severely disabled.

• Excessive sleepiness
• Seizures – generalised tonic clonic type
• Age-related epileptic encephalophy, with seizure onset occurring within the first three months (and often first 10 days) of life. Many, but not all, cases of OS evolve into other seizure disorders, namely West Syndrome and Lennox-Gastaut Syndrome.^[1]

Infant is very floppy and excessively sleepy.

• Generalized seizures
• Tonic seizures (a generalized seizure involving a sudden stiffening of the limbs).^[3]
• Partial seizures
• Myoclonic seizures
• Profound mental and physical retardation
• Encephalopathy

• OS is characterized by a “burst suppression” pattern
• High voltage spike wave discharge followed by little brain wave activity.^[1]

Treatment outlook is poor. Anti-epileptic drugs and steroids may be used to try to control the seizures, but their effectiveness is limited. Most therapies are related to symptoms and day-to-day living. Few infants with focal lesions can have surgery to correct underlying abnormality.

Template:WikiDoc Sources