Alexander disease
What are the symptoms?
The onset of Alexander disease may occur at any time during infancy or adulthood. For many individuals onset is between birth and two years, with the average being six months. This infantile form of the disease affects boys and girls and leads to delayed development and dementia. The condition is characterised by an enlarged brain and head (megalencephaly), progressive spasticity (stiffness of the arms and/or legs), cerebellar ataxia and dementia. Infants fail to thrive, show delayed mental and physical development, and have seizures. Hydrocephalus may occur. Sadly, the outlook is generally poor and children rarely survive past the age of five to six years.
Background
| What are the causes? ![]()