An unusual phenotype of spinocerebellar ataxia type 12
Objective: To describe a case of spinocerebellar ataxia type 12 (SCA-12) with an unusual phenotype. Background: SCA-12 is a rare autosomal dominant cerebellar ataxia which…Amantadine-induced negative myoclonus in a patient with Parkinson’s disease: A case report
Objective: To report a case of amantadine-induced negative myoclonus in a patient with Parkinson’s disease. Background: Parkinson’s disease is a progressive neurodegenerative disease that involves…The distinct EEG signature of celiac disease-related cortical myoclonus
Objective: To describe a novel motor cortex (M1) electroencephalogram (EEG) abnormality distinct to celiac disease (CD)-related cortical myoclonus and to explore its relationship with cerebellar-M1…Adult-Onset Parainfectious Opsoclonus-Myoclonus: Report of Two Cases
Objective: Present two cases of Adult-Onset parainfectious Opsoclonus-Myoclonus Syndrome with fast and good recovery Background: Adult-Onset Opsoclonus-Myoclonus (AOMS) is a rare disorder. Two main causes…Steroid-responsive myoclonus in the context of pembrolizumab treatment: a novel neurological phenotype.
Objective: To outline a novel immunologically-mediated neurological adverse event associated with the use of a medication class which has an expanding range of applications [1].…High dose amantadine therapy may cause increased falling in Parkinson’s patients
Objective: To report a possible association between high dose amantadine and increased falling in patients with Parkinson’s disease (PD). Background: Amantadine is used in PD…A retrospective analysis of clinical and electrophysiological characteristics of patients with myoclonus
Objective: We aimed to evaluate the clinical characteristics of patients with myoclonus and to identify the possible etiologies in different types of myoclonus based on…Generalised Polymyoclonus In a Patient With Central Nervous System Tuberculosis
Objective: Myoclonus associated with tuberculosis or following an infectious event is a transient event with an abrupt onset. It is a rare phenomenon and often…Dancing larynx syndrome associated with trigeminal neuralgia secondary to multiple sclerosis
Objective: To describe a rare a case of a patient who developed “dancing larynx”-like syndrome after gamma knife radiation for trigeminal neuralgia (TN) associated with…A novel intronic pentanucleotide TTTGA repeat insertion in SAMD12 causes familial cortical myoclonic tremor with epilepsy type 1
Objective: To identify the genetic cause in a familial cortical myoclonic tremor with epilepsy (FCMTE) pedigree without reported pathogenic(TTTCA)n insertions. Background: FCMTE is an autosomal…
Abstracts from the International Congress of Parkinson’s and Movement Disorders.