Subacute Sclerosing Panencephalitis

Below you will find more information about Subacute Sclerosing Panencephalitis from Medigest. If you believe that you are suffering from any of the symptoms of Subacute Sclerosing Panencephalitis it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Subacute Sclerosing Panencephalitis and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Subacute Sclerosing Panencephalitis comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Subacute sclerosing panencephalitis (SSPE) is a rare chronic, progressive encephalitis that mainly affects children and young adults, caused by a persistent infection of immune resistant measles virus.


Diagnosis of SSPE is often difficult due to a normal CSF profile - noted changes in the CSF profile only include a marked elevation in CSF immunoglobulin.


There is no cure for SSPE but if it is caught early then the sufferer can respond to the treatment and prevent symptom recurrence by taking the medication for the rest of their life.

Symptoms and Signs

It is marked by a history of primary measles infection before the age of 2 years, followed by several asymptomatic years (6-15 on average), and then gradual, progressive psychoneurological deterioration, consisting of personality change, seizures, myoclonus, ataxia, photosensitivity, ocular abnormalities, spasticity, and coma.

Discuss Subacute Sclerosing Panencephalitis in our forums

Discuss Subacute Sclerosing Panencephalitis with other members of Medigest in our forums.