Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Inherited ataxia with slow saccades.

Journal of postgraduate medicine - 1 Jan 2000

Chakor R T, Bharote H

Abstract excerpt

Ataxia is a symptom of cerebellar dysfunction. Slowly progressive ataxia, dysarthria in an adult with a positive family history suggests an inherited cerebellar ataxia. We present an adult with gradually progressive ataxia and slow saccades. There was history of similar illness in his son. Genetic testing for spinocerebellar ataxia 2 was positive. We discuss the various inherited ataxias, causes of acute,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Magnetic Resonance Imaging
Share to Mutation
Share to Polymerase Chain Reaction

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Saccades

Share to Spinocerebellar Ataxias

Source

Identifiers

PMID: 23298936
DOI: 10.4103/0022-3859.105471

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Inherited ataxia with slow saccades.PMID 23298936Read ↗

Genetic cerebellar ataxias.Semantic proximity Read ↗

Cerebellar ataxias.Semantic proximity Read ↗

The inherited cerebellar ataxias: an update.Semantic proximity Read ↗

Clinical features and molecular genetics of autosomal recessive cerebellar ataxias.Semantic proximity Read ↗

The spinocerebellar ataxias.Semantic proximity Read ↗

Inherited ataxias.Semantic proximity Read ↗

Clinical features and natural history of spinocerebellar ataxia type 1.Semantic proximity Read ↗

Slow saccades and other eye movement disorders in spinocerebellar atrophy type 1.Semantic proximity Read ↗

Hereditary ataxias and paediatric neurology: new movers and shakers enter the field.Semantic proximity Read ↗

More Than Ataxia: Hyperkinetic Movement Disorders in Childhood Autosomal Recessive Ataxia SyndromesSemantic proximity Read ↗

[The autosomal dominant cerebellar ataxias are hereditary neurodegenerative diseases].Semantic proximity Read ↗

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.