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

Hereditary Spastic Paraplegia Type 11-Clinical, Genetic and Neuroimaging Characteristics.

International journal of molecular sciences - 15 Dec 2023

Chojdak-Łukasiewicz Justyna, Sulima Katarzyna, Zimny Anna, Waliszewska-Prosół Marta, Budrewicz Sławomir

Abstract excerpt

Hereditary spastic paraplegia (HSP) is a heterogeneous group of genetically determined diseases, characterised by progressive spastic paraparesis of the lower limbs, associated with degeneration of the corticospinal tract and the posterior column of the spinal cord. HSP occurs worldwide and the estimated prevalence is about 1-10/100,000, depending on the geographic localisation. More than 70 genes responsible for...

Read the complete abstract on PubMed

Topics

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

Share to Hereditary Neurological Disorders
Share to Mitochondria

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Neurogenetic and Muscular Disorders Research

Share to Neuroimaging

Share to Neurological diseases and metabolism

Share to Pyramidal Tracts

Share to Spastic Paraplegia, Hereditary

Source

Open in PubMed Open full text

Identifiers

PMID: 38139357
DOI: 10.3390/ijms242417530
PMCID: PMC10743703

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hereditary Spastic Paraplegia Type 11-Clinical, Genetic and Neuroimaging Characteristics.PMID 38139357Read ↗

Insights into Clinical, Genetic, and Pathological Aspects of Hereditary Spastic Paraplegias: A Comprehensive OverviewSemantic proximity Read ↗

French guidelines for the diagnosis and management of pure hereditary spastic paraplegiaSemantic proximity Read ↗

Genetics of hereditary spastic paraplegias.Semantic proximity Read ↗

Clinical features and management of hereditary spastic paraplegia.Semantic proximity Read ↗

Hereditary spastic paraparesis: The real-world experience from a Neurogenetics outpatient clinic.Semantic proximity Read ↗

Hereditary Spastic Paraplegia: An Update.Semantic proximity Read ↗

Clinical and genetic study of hereditary spastic paraplegia in CanadaSemantic proximity Read ↗

Hereditary spastic paraplegia type 11: Clinicogenetic lessons from 339 patients.Semantic proximity Read ↗

An Update on the Hereditary Spastic Paraplegias: New Genes and New Disease ModelsSemantic proximity Read ↗

Revisiting genotype-phenotype overlap in neurogenetics: triplet-repeat expansions mimicking spastic paraplegias.Semantic proximity Read ↗

Paediatric-onset hereditary spastic paraplegias: a retrospective cohort study.Semantic proximity Read ↗

Hereditary spastic paraplegia.Semantic proximity Read ↗

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