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…Improvement in chorea and function in a patient with dystonia-choreoathetosis cerebral palsy after treatment with bilateral pallidal deep brain stimulation
Objective: We describe and demonstrate by video a patient with dystonia-choreoathetosis cerebral palsy treated with bilateral pallidal deep brain stimulation (DBS). Background: Dystonia-choreoathetosis cerebral palsy…Deep brain stimulation for choreoathetosis in cerebral palsy: Pallidal versus thalamic stimulation
Objective: We aimed to assess, whether the thalamic ventral intermediate nucleus (Vim) might be an alternative target for DBS in choreoathetosis. Background: Choreoathetosis is common…Choreaathetosis as clinical manifestation of Fahr Syndrome inTurner Syndrome Patient
Objective: To report choreaathetosis as a clinical manifestation of Fahrs syndrome in Turner Syndrome patient Background: The prevalence of fahr syndrme is 1/1000.000 people. Clinical…Generalized choreoathetoid-like movements in primary Sjögren syndrome
Objective: To report a case of choreoathetoid-like movements associated to primary Sjögren syndrome. Background: Autoimmune diseases are not uncommon causes of movement disorders. Two percent…Acute concomitant presentation of chorea and subacute combined degeneration secondary to vitamin B12 deficiency
Objective: To describe an exceptional presentation of vitamin B12 deficiency. Background: Vitamin B12 deficiency typically presents with subacute combined degeneration (SCD). Extrapyramidal symptoms are rare,…Neuroferritinopathy pedigree in 2 families from India
Objective: The abstract provides description of first case report of two Indian families with Neuroferritinopathy (NFT) pedigree. Background: NFT is a rare autosomal dominant movement disorder caused…Fentanyl Induced Chorea: A Case Report
Objective: To report the acute onset of generalized chorea as an adverse reaction to transdermal fentanyl Background: Chorea can present with degenerative conditions or in an…
Abstracts from the International Congress of Parkinson’s and Movement Disorders.