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

The unique co-occurrence of spinocerebellar ataxia type 10 (SCA10) and Huntington disease.

Journal of the neurological sciences - 15 Jan 2013

Roxburgh Richard H, Smith Corrie O, Lim Jung G, Bachman David F, Byrd Erica, Bird Thomas D

Abstract excerpt

We present a unique thirty-nine year old woman with both Huntington's disease (HD) and spinocerebellar ataxia type 10 (SCA10). She has 48 CAG repeats in the HD gene and 2511 ATTCT repeats in the ATX10 gene. Although both conditions are repeat expansion diseases they are thought to have quite different pathogenic mechanisms. The symptomatic age of onset in this patient (mid30s) is within the expected range for her...

Read the complete abstract on PubMed

Topics

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

Share to Cognition
Share to Depression
Share to DNA Repeat Expansion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Huntington Disease

Share to Indians, South American

Share to Psychiatric Status Rating Scales

Share to Spinocerebellar Ataxias

Share to Wechsler Scales

Source

Identifiers

PMID: 23083689
DOI: 10.1016/j.jns.2012.09.030

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The unique co-occurrence of spinocerebellar ataxia type 10 (SCA10) and Huntington disease.PMID 23083689Read ↗

First report of a Japanese family with spinocerebellar ataxia type 10: The second report from Asia after a report from China.Semantic proximity Read ↗

Spinocerebellar ataxia type 10: a disease caused by a large ATTCT repeat expansion.Semantic proximity Read ↗

Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestry.Semantic proximity Read ↗

Understanding the dynamics of Spinocerebellar Ataxia 8 (SCA8) locus through a comparative genetic approach in humans and apes.Semantic proximity Read ↗

Allelic Diversity, de novo CAG Expansions, and Intergenerational Instability at the HTT Locus in a clinical sample of Huntington’s Disease from IndiaSemantic proximity Read ↗

Complexity of the Genetics and Clinical Presentation of Spinocerebellar Ataxia 17Semantic proximity Read ↗

A new mutation for Huntington disease following maternal transmission of an intermediate allele.Semantic proximity Read ↗

Simultaneous ALS and SCA2 associated with an intermediate-length ATXN2 CAG-repeat expansionSemantic proximity Read ↗

Incidence and mutation rates of Huntington's disease in Spain: experience of 9 years of direct genetic testing.Semantic proximity Read ↗

Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan.Semantic proximity Read ↗

"A case report: Co-occurrence of cerebral amyloid angiopathy and multiple sclerosis".Semantic proximity Read ↗

Two in one: report of a patient with spinocerebellar ataxia types 2 and 10.Semantic proximity Read ↗

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