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Published on: July 10, 2013
Juvenile neuronal ceroid lipofuscinosis (Batten disease): current insights
1Department of Paediatrics, Aarhus University Hospital, Centre for Rare Diseases, Aarhus, Denmark, john.oestergaard@skejby.rm.dk.
Insights
Juvenile Neuronal Ceroid Lipofuscinosis (JNCL), caused by CLN3 mutations, progressively impacts vision, cognition, and motor skills. This review details the debilitating symptoms and typical disease progression in patients with JNCL.
Area of Science:
- Neuroscience
- Genetics
- Pediatric Neurology
Background:
- Juvenile Neuronal Ceroid Lipofuscinosis (JNCL), also known as Batten disease, is a rare genetic disorder.
- Mutations in the CLN3 gene are a primary cause of JNCL, leading to progressive neurodegeneration.
Purpose of the Study:
- To provide a comprehensive overview of the clinical manifestations and progression of JNCL caused by CLN3 mutations.
- To highlight the multifaceted impact of JNCL on vision, cognition, behavior, motor function, and cardiac health.
Main Methods:
- This is a review article, synthesizing existing research and clinical observations.
- The review focuses on the natural history and symptom progression of JNCL based on published literature.
Main Results:
- Vision impairment typically begins around 5-6 years of age, followed by cognitive decline and behavioral issues.
- Seizures, motor deficits (ataxia, extrapyramidal symptoms), and swallowing difficulties emerge progressively.
- Cardiac involvement and severe dementia occur in adolescence, leading to profound disability and early mortality, usually by the third decade.
Conclusions:
- CLN3-related JNCL is a devastating neurodegenerative disease with a predictable but severe progression.
- Early identification and understanding of JNCL's complex symptoms are crucial for patient care and future therapeutic strategies.
Abstract:
The present review is focused on juvenile neuronal ceroid lipofuscinosis (JNCL; Batten disease) due to a mutation in CLN3. Functional vision impairment occurring around 5-6 years of age is the first symptom in more than 80% of patients. Approximately 2 years later (though sometimes simultaneously), obvious signs of cognitive impairment appear. Behavior problems can occur in advance, especially in boys. These include anxious and depressed mood, aggressive behavior, and hallucinations, and even psychotic symptoms. Following the teens, severe dementia is present, including loss of memory, attention, and general reasoning abilities, as well as loss of independent adaptive skills such as mobility, feeding, and communicating. Sleep abnormalities, such as settling problems, nocturnal awakenings, and nightmares, are reported in more than half of patients. The vast majority, if not all, patients develop seizures, starting at approximately 10 years of age. Generalized tonic-clonic seizure occurs as the only type of seizure in approximately half of patients, and in combination with partial seizures in a third of patients. There seems to be no difference in seizure severity according to sex or genotype, and there is great variation in seizure activity among patients. Soon after diagnosis, patients begin to have slight ataxic symptoms, and at adolescence extrapyramidal symptoms (rigidity, bradykinesia, slow steps with flexion in hips and knees) occur with increasing frequency. Chewing and swallowing difficulties emerge as well, and food intake is hampered in the late teens. Disabling periodically involuntary movements may occur as well. A progressive cardiac involvement with repolarization disturbances, ventricular hypertrophy, and sinus-node dysfunction, ultimately leading to severe bradycardia and/or other conduction abnormalities, starts in the mid-teens. Patients are usually bedridden at 20 years of age, and death usually occurs in the third decade of life.
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