Leukoencephalopathy
Leukoencephalopathy is a term that describes all of the brain white matter diseases, whether their molecular cause is known or unknown. It can refer specifically to any of these diseases:
- Progressive multifocal leukoencephalopathy
- Toxic leukoencephalopathy
- Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
- Leukoencephalopathy with vanishing white matter
- Leukoencephalopathy with neuroaxonal spheroids
- Reversible posterior leukoencephalopathy syndrome
- Megalencephalic leukoencephalopathy with [subcortical cysts]. It can also refer to gene MLC1 or Megalencephalic leukoencephalopathy with subcortical cysts 1, a human gene related to the former disease.
- Hypertensive leukoencephalopathy
The acquired demyelinating diseases are classified according to their underlying causes into five groups: noninfectious–inflammatory, infectious–inflammatory, toxic–metabolic, hypoxic–ischemic, and traumatic.
This classification is diffuse sometimes. For example CADASIL syndrome is at the same time hereditary and hypoxic.