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. 2020 Apr 24;56(8):1210–1218. doi: 10.1111/jpc.14890

Figure 1.

Figure 1

Path to diagnosis for CLN2 disease is through a combination of enzymatic and genetic investigations after initial suspicion is raised. CLN2, ceroid lipofuscinosis type 2; EEG, electroencephalogram; MRI, magnetic resonance imaging; TPP1, tripeptidyl peptidase 1.