Children with CLN2 disease

Clinical Evaluations

EEG with low-frequency intermittent photic stimulation and other clinical tests can be used to detect CLN2 disease1,2

The majority of children with CLN2 disease have been reported to show a response to low-frequency intermittent photic stimulation (IPS).3

EEG with IPS

EEG with low-frequency IPS can be used to detect photo sensitivity in children with CLN2 disease

  • A photoparoxysmal response (PPR) is common in patients with CLN2 disease and has features that are distinguishable from PPRs seen in other epilepsies3
  • Low-frequency (1-2 Hz) IPS induces the appearance of time-locked high-amplitude occipital spikes in many cases3,4
  • Positive PPR should be followed by enzymatic and/or molecular testing to rule out NCL4
  • Not all children with CLN2 disease will exhibit this response. Performing diagnostic enzymatic and/or molecular tests will rule out or confirm CLN2 disease if suspected3,4
Electroencephalogram (EEG) assessment
EEG used with permission from Nicola Specchio, MD, PhD.
Many children with CLN2 disease show a photoparoxysmal response or a pathognomonic response to EEG with low-frequency (1-2 Hz) IPS.3

Other clinical assessments may provide findings indicative of CLN2 disease, including:

Brain MRI

Early in the disease, a brain MRI may appear normal or show subtle abnormalities. Abnormalities that should raise the level of suspicion for CLN2 disease include1,2:

  • Cerebellar atrophy, which is a common finding in NCLs
  • Periventricular white matter hyperintensity

Later in the disease, cerebral atrophy becomes evident and will progress.1,2

Brain MRI

Worgall S. et al. Neurology. 2007 Aug 7;69(6):521-35.

Ophthalmological assessments

Though blindness occurs late in the progression of CLN2 disease, visual abnormalities may be identified using certain ophthalmologic assessments.5

Note: This image is from a 8-year-old patient, reflecting late stage advances of CLN2 disease.6

Optical coherence tomography (OCT)

OCT can demonstrate progression of CLN2 disease via retinal degeneration and accumulation of hyper-reflective material.6,7

Fluorescein angiography (FA)

FA can be used to evaluate vascular leakage.6

Visual evoked potential (VEP)

VEPs are abnormally enhanced until late in the disease and diminish in the final stage of the disease.1

Electroretinogram (ERG)

ERG may be diminished before visual deterioration is clinically detected.1,2

Additional clinical tests used to identify CLN2 disease

Electron microscopy (EM)

Although the use of electron microscopy in clinical practice has decreased worldwide, it is used to detect the distinct curvilinear structure of ceroid lipofuscin in suspected cases, often when other tests are inconclusive.5

There are a number of clinical tests that can help identify CLN2, but only enzymatic and/or molecular testing can definitively diagnose CLN2 disease.

References: 1. Chang M, Cooper JD, Davidson BL, et al. CLN2. In: Mole S, Williams R, and Goebel H, eds. The neuronal ceroid lipofuscinoses (Batten Disease). 2nd ed. Oxford, United Kingdom: Oxford University Press; 2011:80-109. 2. Mole SE, Williams RE, and Goebel HH. Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses. Neurogenetics. 2005;6:107-126. 3. Albert DV, Yin H, De Los Reyes EC, Vidaurre J. Unique Characteristics of the photoparoxysmal response in patients with neuronal ceroid lipofuscinosis type 2: can EEG be a biomarker? [Epub ahead of print July 21, 2016]. J Child Neurol. DOI: 10.1177/0883073816658659. 4. Fietz M, AlSayed M, Burke D, et al. Diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2 disease): Expert recommendations for early detection and laboratory diagnosis. [Epub ahead of print July 25, 2016]. Mol Genet Metab. doi: 10.1016/j.ymgme.2016.07.011. 5. Mole SE, Williams RE. Neuronal ceroid-lipofuscinoses. 2001 Oct 10 [Updated 2013 Aug 1]. In: Pagon RA, Adam MP, Ardinger HH, et al., editors. GeneReviews® [internet]. Seattle, WA: University of Washington; 1993-2016. 6. Orlin A, Sondhi D, Witmer MT, et al. Spectrum of ocular manifestations in CLN2-associated Batten (Jansky-Bielschowsky) Disease correlate with advancing age and deteriorating neurological function. PLoS One. 2013;8:e73128. doi:10.1371/journal.pone.0073128. 7. Williams RE, Adams HR, Blohm M, et al. Expert opinion on the management of CLN2 disease. Poster session presented at: The 12th Annual WORLD Symposium; February – March 2016; San Diego, CA.