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. 2018 Jan 10;5(2):149–155. doi: 10.1002/mdc3.12573

Figure 1.

Figure 1

A: Distribution of different lysosomal storage diseases (LSD) in this cohort of 76 patients with a clinical, genetic and/or biochemical diagnosis of a LSD. B: Summary of 18 LSD patients who presented with at least one of the predefined movement disorders (parkinsonism, dystonia, ataxia, tremor, chorea, myoclonus, ballism, restless leg syndrome). C: Distribution of 36 movement disorders in these 18 patients. Abbreviations: AG, aspartylglycosaminuria; CLN, ceroid lipofuscinosis; MPS, mucopolysaccharidosis.