Long term follow-up of cerebrovascular abnormalities in late onset Pompe disease (LOPD).

The article discusses a study which described intracranial artery abnormalities in patients with late onset Pompe disease (LOPD) or glycogen storage disease type II. Topics include the causes and clinical characteristics of LOPD, the role of enzyme replacement therapy (ERT) in improving the condition of patient with LOPD, and an overview of the radiological data of the long-extended term follow-up of a cohort of LOPD Pome patients studied between 2006 and 2016.