Novel GNO1 mutation in monozygotic twins responsive to DBS
Objective: GNAO1 is located on chromosome 16q12.2 and encodes Gα0 subunit of the heterotrimeric guanine-binding protein necessary for neuronal signaling. It is thought that loss-of-function GNAO1…Can Handwriting Movement Abnormalities Serve as an Early Biomarker of Transition to Manifest Huntington’s disease?
Objective: The objective of this study was to examine whether handwriting abnormalities are present prior to clinically manifest chorea in Huntington's disease (HD) and can…The clinical spectrum of movement disorders associated with neuronal antibodies
Objective: To describe the clinical and treatment characteristics of movement disorders associated with antibodies (Abs) against neuronal synaptic extracellular (NMDAR, LGI1, CASPR2, IgLON5, Glycine receptors…Knowledge and attitude towards movement disorders among final year medical students in a Nigerian university
Objective: The study was aimed to evaluate knowledge and attitude of medical students towards movement disorders. Background: The understanding of movement disorders could pose a…MOVEMENT DISORDERS FEATURES ASSOCIATED WITH WEST SYNDROME
Objective: To describe the clinical, therapeutic and outcome features of movement disorders (MD) observed in children with West Syndrome (WS) at the Neurology Department of…Acute chorea secondary to cephalosporin
Objective: To report a case of acute chorea induced by ceftriaxone and to explain neurotoxicity of antibiotics. Background: B Chorea was classically described in patients…Post-pump chorea and progressive supranuclear palsy like syndrome following major cardiac surgery: A case series
Objective: We report three patients who developed movement disorders after major cardiac surgery and suggest a common underlying mechanism. Background: Choreiform movement disorder occurs in…Movement disorders associated with autoimmune encephalitis
Objective: We aim to highlight the spectrum of movement disorders in patients of autoimmune encephalitis (AE) diagnosed at our tertiary care center and describe their…PRRT2 mutations are associated with a wide intrafamilial ad interfamilial phenotypic variability
Objective: To describe the different clinical syndromes associated with PRRT2 mutations in two different families Background: Mutations in the Proline-Rich Transmembrane Protein 2 (PRRT2) gene…Crack Dancing: An Uncommon Drug-Induced Chorea
Objective: To report a unique case of cocaine induced choreiform dyskinetic movements with literature review of this condition. Background: Various abnormal movements have been known…