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Pediatric Rasmussen syndrome causes inflammation on one side of the brain and seizures.
214-456-2768
Fax: 214-456-6898
469-303-0055
Fax: 469-303-0655
Rasmussen's syndrome (Rasmussen encephalitis), a type of encephalitis, is a very rare form of brain malformation that may happen anytime during childhood.
While the cause is unknown, the disorder causes inflammation in one half of a child's brain. The inflammation affects the nerve cells in the brain and causes seizures. These seizures occur very frequently, often many times a day. Seizures usually start between 14 months and 14 years of age. Weakness and other neurological problems often begin 1 to 3 years after the seizures start.
If the seizure lasts for more than five minutes or seems violent, call 911.
Seizures are usually the first symptom that a child has Rasmussen syndrome. The symptoms a child experiences with this condition depend on which side of their brain is affected.
Possible pediatric Rasmussen syndrome symptoms include:
To diagnose Rasmussen syndrome, your physician will do a detailed physical exam of your child, which will include an electroencephalogram (EEG). An EEG is performed by placing electrodes on the scalp and recording the electrical activity of the brain.
There is no known cause for Rasmussen syndrome.
The seizures associated with Rasmussen syndrome can be difficult to control with medication. Some children benefit from immunomodulatory therapy and others from surgery to disconnect or remove the section of brain causing the seizures.
Rasmussen syndrome causes inflammation in one half of a child's brain. The inflammation affects the nerve cells in the brain and causes seizures.
Epilepsy is a condition that affects how the nerve cells in the brain communicate with each other. When the normal electrical activity in the brain interferes with this communication process, seizures can occur.
The epilepsy symptoms most people recognize are shaking (called convulsions) combined with the body getting rigid, clenching the jaw, and biting the tongue. These are called tonic-clonic seizures and many people still know them as grand mal seizures. But some seizures are barely noticeable.
Children may stare into space, stop talking abruptly and then start talking again, or start repetitious movements like chewing their lips or moving a hand. These types of seizures are called absence seizures, which used to be known as petit mal seizures. Sometimes a child may experience smelling something that isn't there, numbness or a tingling sensations before the seizure. These are called auras.
If the seizure is small twitching or staring, they should come out of it easily. For convulsions, make sure your child is in a chair that they can't fall out of or lying on the floor with a pillow under their head. Turn their head to the side, but NEVER try to put anything into their mouth. Do not shake or hit them or shout at them. If the seizure lasts for more than five minutes or seems violent, call 911.
After a seizure, your child may be confused, foggy or tired. If they want to lie down, let them.
To diagnose Rasmussen syndrome, your physician will do a detailed physical exam of your child, as well as an EEG and brain imaging.
Treatment is focused on controlling the seizures. These seizures may be difficult to control with medication, but surgery has shown more promise.
Our Epilepsy Center will provide you with resources to help both you and your child. The Resources link on this webpage is also a good source for more information about epilepsy and support groups.