Conditions / Genetic
neuronal ceroid lipofuscinosis 9
info · Genetic · ICD-10: E75.4
A neuronal ceroid lipofuscinosis that is characterized by juvenile-onset of progressive vision loss, progressive ataxia and seizures.
Signs and symptoms
- Scanning speech
- Mutism
- Cerebral atrophy
- Seizure
- Dysarthria
- Rigidity
- Ataxia
- Psychomotor deterioration
- Progressive visual loss
- Vacuolated lymphocytes
Also known as: CLN9