adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (Q63860020)
Jump to navigation
Jump to search
leukodystrophy that is characterized by progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy and has material basis in heterozygous mutation in the CSF1R gene on chromosome 5q32
- hereditary diffuse leukoencephalopathy with spheroids
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | adult-onset leukoencephalopathy with axonal spheroids and pigmented glia |
leukodystrophy that is characterized by progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy and has material basis in heterozygous mutation in the CSF1R gene on chromosome 5q32 |
|
Statements
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference