Alexander disease is a rare genetic disorder that affects the nervous system and leads to changes in physical and psychological characteristics. For instance, a usual enlargement of the head or spasticity can be some of the common indicators of the disease. It is rarely found in adults and mostly affects infants & children.
HOW IS ALEXANDER DISEASE DIAGNOSED?
CT scan, MRI scan and genetic testing are the best methods to diagnose Alexander disease.
HOW IS ALEXANDER DISEASE TREATED?
There is currently no cure or standard procedure for treating Alexander disease. However, patients are advised to seek pediatric and neurological expertise.
DID YOU KNOW?
A bone marrow transplant was attempted on a patient, but it remained unsuccessful and could not cure the child.