Delayed progressive spastic cerebellar ataxia and cerebellar atrophy after Heat Stroke
Objective: To describe a very rare case of delayed progressive spastic cerebellar ataxia after an episode of survival after heat stroke Background: Heat stroke is…Ataxia, opsoclonus and peripheral neuropathy induced by chronic toluene intoxication.
Objective: To report a case of a young patient with opsoclonus, ataxia and peripheral neuropathy due to toluene intoxication. Background: Amid the causes of…Ataxia asociated to neuromyelitis optica spectrum disorder
Objective: To describe a case of severe ataxia associated with neuromyelitis optica spectrum disorder with spinal cord and medulla oblongata involment. Background: Although brain stem…The diagnostic dilemma of olivopontocerebellar atrophy and spinocerebellar ataxia, a comparative analysis of clinical cases.
Objective: . Clinical practice often confronts us with ambiguous and conflicting data from the "western" and "eastern" publications, which leads to misunderstandings and disagreements, so…Progressive ataxia and palatal tremor: 2 autopsy cases of a novel tauopathy
Objective: We report clinical and neuropathological findings in 2 cases of sporadic progressive ataxia and palatal tremor (PAPT). Background: Sporadic PAPT is a rare syndrome characterized by mid-…Cerebellar Ataxia – The First Symptom of HIV Infection
Objective: To describe a patient with unusual and rare initial presentation of HIV infection – a progressive cerebellar ataxia. Background: Isolated cerebellar degeneration in an…99mTc -TRODAT- 1 SPECT SHOWING DOPAMINERGIC DEFICIENCY IN A PATIENT WITH SPINOCEREBELLAR ATAXIA TYPE 10 AND PARKINSONISM.
Objective: In this report, we describe a Brazilian patient with SCA10, with parkinsonism, with a 99Tc - TRODAT-1 SPECT demonstrating dopaminergic deficiency. Background: Spinocerebellar ataxia…Spinocerebellar Ataxia type 11 in a Hispanic Kindred
Objective: To present the clinical profiles of two siblings with SCA11 who are of Hispanic origin. Background: Spinocerebellar ataxia type 11 (SCA11) is an autosomal…Eye Movements in Huntington Disease Like 2
Objective: ObjectiveTo determine if eye movements are preserved in Huntington Disease-Like 2 (HDL2) and if this can be used to differentiate HDL2 from Huntington Disease…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…
Abstracts from the International Congress of Parkinson’s and Movement Disorders.