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

Slowed vertical saccades as a hallmark of hereditary spastic paraplegia type 7

1 Oct 2019

Abstract excerpt

Anecdotal oculomotor disturbances have been described in spastic paraplegia type 7 (SPG7). We investigated oculomotor and vestibular dysfunction in five patients with genetically verified SPG7. All five patients exhibited significantly slower velocities of vertical saccades compared to controls, but significantly faster than in progressive supranuclear palsy, with upward saccades being particularly affected....

Read the complete abstract on PubMed

Topics

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

Share to Botulinum Toxin and Related Neurological Disorders
Share to Hereditary Neurological Disorders
Share to Neurological diseases and metabolism

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 31602813
DOI: 10.1002/acn3.50907

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Slowed vertical saccades as a hallmark of hereditary spastic paraplegia type 7PMID 31602813Read ↗

Ocular motor biomarkers in Niemann-Pick disease type C: A prospective cross-sectional multicontinental study in 72 patientsSemantic proximity Read ↗

Neurophysiological and ophthalmological findings of SPG7-related spastic ataxia: a phenotype study in an Irish cohort.Semantic proximity Read ↗

Spastic Paraplegia Type 7 and Movement Disorders: Beyond the Spastic ParaplegiaSemantic proximity Read ↗

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

Ocular Motor and Vestibular Profile in Spinocerebellar Ataxia Type 27B: Toward a Practical Bedside Diagnostic FrameworkSemantic proximity Read ↗

Genotype-phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort.Semantic proximity Read ↗

Oculomotor phenotypes in autosomal dominant ataxias.Semantic proximity Read ↗

Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA17).Semantic proximity Read ↗

Abnormal Vertical Eye Movements as a Clue for Diagnosis of Niemann-Pick Type C.Semantic proximity Read ↗

Inherited ataxia with slow saccades.Semantic proximity Read ↗

Spastic Paraplegia Type 7-Associated Optic Neuropathy: A Case Series.Semantic proximity Read ↗

Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia.Semantic proximity Read ↗

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