Related Experiment Video
Updated: Jan 31, 2026

High-speed Video Microscopy Analysis for First-line Diagnosis of Primary Ciliary Dyskinesia
Published on: January 19, 2022
Paroxysmal Dyskinesias in a PRRT2 Mutation Carrier
Massimo Marano1, Francesco Motolese1, Federica Consoli2
1Neurology, Neurophysiology and Neurobiology Unit, Department of medicine, Campus Bio-Medico of Rome University, Rome, IT.
Background:
Paroxysmal movement disorders are rare and heterogeneous genetic conditions characterized by the recurrence of transient involuntary movements.
Phenomenology Shown:
The phenomenology of a paroxysmal kinesigenic dyskinesia in a young professional athlete.
Educational Value:
Providing basic clinical and genetic elements for the early recognition and diagnosis of a rare movement disorder.
More Related Videos
Related Concept Videos
Electron Carriers
Over the many stages of cellular respiration, glucose breaks down into carbon dioxide and water. Electron carriers pick up electrons lost by glucose in these reactions, temporarily storing and releasing them into the electron...
Mutations
Mutations
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
Viral Mutations
Carrier Transport
Drift Current:
The drift of charge carriers is started by an external electric field (E). Charged particles, such as electrons and holes, experience an acceleration between collisions with lattice atoms. For electrons, this results in a drift velocity (vd) given by:
Mutation, Gene Flow, and Genetic Drift

