Functional Movement Disorder and Parkinson’s Disease Comorbidity: A Case Report

Case Presentation A 22-year-old male patient presented to the emergency room of hospital with chief complaints of restlessness, an intolerable urge to pace around, suspiciousness, and sleep disturbances in the form of late-onset and midnight awakenings for four days. Medical History Family History Clinical Exam Treatment Clinical Outcome Careful observation, interviews, and periodic mental status […]

Parkinsonism caused by adverse drug reactions

A 29-year-old Nigerian Edo woman, presented with a five-day history of tremor of her fingers and head at rest, with associated drooling of saliva from her mouth. There was no history of fever, vomiting, headache, dyspeptic symptoms, or any other neurological symptoms, although she reported dizziness. She had not used any drugs in the preceding […]

Lack of association between PLA2G6 genetic variation and Parkinson’s disease: a systematic review

INTRODUCTION: The phospholipase A2 Group 6 (PLA2G6, also known as PLA2, PARK14, and iPLA2) gene encodes a group via calcium-independent phospholipase A2. Genetic polymorphism of PLA2G6 has been indicated to be involved in conferring susceptibility for Parkinson’s disease (PD), whereas conclusive results have not been obtained.  OBJECTIVE: To conduct a systematic review to determine if PLA2G6 genetic variation confers greater susceptibility […]