Paroxysmal Non‐Kinesigenic Dyskinesia: Utility of the Quantification of GLUT1 in Red Blood Cells

Glucose transporter type 1 deficiency syndrome (Glut1DS) is a treatable genetic neurometabolic disorder because of a variant in the Glut1 transporter, encoded by the SLC2A1 gene (OMIM*138140), resulting in impaired glucose transport across the blood–brain barrier. Glut1DS was initially reported in i... View More