Article

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

2022-09-20

Abstract excerpt

<h4>Background: </h4> Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease (MJD), is an autosomal dominant genetic disease with substantial heterogeneity in clinical manifestations. It typically starts with ataxia and can be divided into five subtypes. The fourth subtype of SCA3 is characterized by parkinsonian and peripheral neuropathy. However, this phenotype is rare, and it tends to be eas...

Topics

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

Identifiers and source

Literature Corpus work: 34951c47-e37e-5f97-87c8-f2f61b315291
DOI: 10.21203/rs.3.rs-2069417/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Initially with pure parkinsonian phenotype of spinocerebellar ataxia type 3: A rare case report and literature reviewDOI 10.21203/rs.3.rs-2069417/v1Read

Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case report.Semantic proximity Read

Parkinsonism in Spinocerebellar AtaxiaSemantic proximity Read

"Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide.Semantic proximity Read

Dominantly inherited ataxias: lessons learned from Machado-Joseph disease/spinocerebellar ataxia type 3.Semantic proximity Read

Machado-Joseph Disease: from first descriptions to new perspectives.Semantic proximity Read

[Overview of Hereditary Spinocerebellar Ataxias in Japan].Semantic proximity Read

Machado Joseph disease: clinical and genetic aspects, and current treatmentSemantic proximity Read

[Recent advances in molecular genetics of spinocerebellar ataxia type 3/Machado-Joseph disease].Semantic proximity Read

[Progressive supranuclear palsy; an unusual form of parkinsonism].Semantic proximity Read

[The broad phenotypic spectrum of SCA-3: hereditary spastic paraplegia].Semantic proximity Read

Spinocerebellar Ataxia Type 23 (SCA23): a rare cause of SCA in the AmericasSemantic proximity Read

Spinocerebellar ataxias in Asia: Prevalence, phenotypes and management.Semantic proximity Read