Catalog
Neuronal ceroid lipofuscinosis
Link to WHO Definition
Neuronal ceroid lipofuscinosis – http://id.who.int/icd/entity/1568332253
Neuronal ceroid lipofuscinoses (NCLs) are a group of inherited progressive degenerative brain diseases characterised clinically by a decline of mental and other capacities, epilepsy, and vision loss through retinal degeneration, and histopathologically by intracellular accumulation of an autofluorescent material, ceroid lipofuscin, in the neuronal cells in the brain and in the retina.
Parents
Children
- Cerebral lipidosis myoclonic variant
- Adult neuronal ceroid lipofuscinosis
- Finnish variant of late infantile neuronal ceroid lipofuscinosis
- Juvenile neuronal ceroid lipofuscinosis
- Cerebral lipidoses
- Late infantile neuronal ceroid lipofuscinosis
- Neuronal ceroid lipofuscinosis type 10
- Congenital neuronal ceroid lipofuscinosis
- Cerebroretinal lipidosis
- Infantile neuronal ceroid lipofuscinosis