Articles with "16p11 2md" as a keyword



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Paroxysmal Kinesigenic Dyskinesia Caused by 16p11.2 Microdeletion and Related Clinical Features

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Published in 2022 at "Neurology: Genetics"

DOI: 10.1212/nxg.0000000000000659

Abstract: Background and Objectives Isolated paroxysmal kinesigenic dyskinesia (PKD) is mainly caused by PRRT2 variants and TMEM151A variants. Patients with proximal 16p11.2 microdeletion (16p11.2MD) (including PRRT2) often have neurodevelopmental phenotypes, whereas a few patients have PKD.… read more here.

Keywords: patients pkd; 16p11 2md; 16p11 microdeletion; paroxysmal kinesigenic ... See more keywords