Intracranial arterial abnormalities in patients with late onset Pompe disease (LOPD). Montagnese F, Granata F, Musumeci O, et al. J Inherit Metab Dis 2016; 39:391-398. Abstract Background: Pompe disease is a rare metabolic disorder due to lysosomal alpha-glucosidase (GAA) deficiency. It is considered as a multi-systemic disease since, although glycogen accumulation is largely prominent in […]

via What are the intracranial vascular anomalies of late onset Pompe disease? — Neurochecklists Updates

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