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Article

Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum.

Neuropediatrics - 1 Apr 2006

Olmez A, Uyanik G, Ozgül R K, Gross C, Cirak S, Elibol B, Anlar B, Winner B, Hehr U, Topaloglu H, Winkler J

Abstract excerpt

Hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurodegenerative disorders leading to progressive spasticity of the lower limbs. Clinically, HSPs are divided into "pure" and "complicated" forms. In pure HSP, the spasticity of the lower limbs is the sole symptom, whereas in complicated forms additional neurological and non-neurological features are observed. Genetically, HSPs are divided into...

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Share to Chromosomes, Human, Pair 15
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Source

Identifiers

PMID: 16773502
DOI: 10.1055/s-2006-923982

Genes

SPG11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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