Article

Midbrain atrophy related to parkinsonism in a non-coding repeat expansion disorder: five cases of spinocerebellar ataxia type 31 with nigrostriatal dopaminergic dysfunction

2021-03-06

Abstract excerpt

<title>Abstract</title> <p>Background Spinocerebellar ataxia type 31 (SCA31) is caused by non-coding pentanucleotide repeat expansions in the <italic>BEAN1</italic> gene. Clinically, SCA31 is characterized by late-adult onset, pure cerebellar ataxia. To explore the association between parkinsonism and SCA31, five patients with SCA31 with concomitant nigrostriatal dopaminergic dysfunction (NSDD) development, incl...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 60e328ba-c963-5f63-a9cb-e18afadbbb1d
DOI: 10.21203/rs.3.rs-282156/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Midbrain atrophy related to parkinsonism in a non-coding repeat expansion disorder: five cases of spinocerebellar ataxia type 31 with nigrostriatal dopaminergic dysfunctionDOI 10.21203/rs.3.rs-282156/v1Read

Midbrain Atrophy Related to Parkinsonism in a Non-Coding Repeat Expansion Disorder: Five Cases of Spinocerebellar Ataxia Type 31 With Nigrostriatal Dopaminergic DysfunctionSemantic proximity Read

Parkinsonism in Spinocerebellar AtaxiaSemantic proximity Read

Initially with pure parkinsonian phenotype of spinocerebellar ataxia type 3: A rare case report and literature reviewSemantic proximity Read

Levodopa responsive parkinsonism in Spinocerebellar ataxia 27BSemantic proximity Read

Non-Ataxic Phenotypes of SCA8 Mimicking Amyotrophic Lateral Sclerosis and Parkinson DiseaseSemantic proximity Read

Differential value of brain magnetic resonance imaging in multiple system atrophy cerebellar phenotype and spinocerebellar ataxias.Semantic proximity Read

PSP-Phenotype in SCA8: Case Report and Systemic Review.Semantic proximity Read

Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: Genetic, clinical, and positron emission tomography findingsSemantic proximity Read

Profile of families with parkinsonism‐predominant spinocerebellar ataxia type 2 (SCA2)Semantic proximity Read

Spinocerebellar ataxia type 2 presenting as familial levodopa‐responsive parkinsonismSemantic proximity Read

Differential diagnosis of parkinsonian degenerative disorders in combination manual measurements with automated volumetry of the brainSemantic proximity Read