Novel KIF5A variant in a patient with early-onset levodopa-responsive Parkinson’s syndrome

We present the case of a male in his mid-30s with a progressive complex neurological phenotype primarily characterised by levodopa-responsive parkinsonism with motor fluctuations as well as gait ataxia, peripheral neuropathy and finally also spastic paraplegia. Genetic analysis identified a novel heterozygous variant in the KIF5A gene: c.937G>A (p.Glu313Lys). This variant is genetically classified as likely pathogenic. Other pathogenic mutations in the KIF5A gene are associated with hereditary spastic paraplegia type 10, Charcot-Marie-Tooth disease type 2 and amyotrophic lateral sclerosis. We discuss the clinical, genetic and prognostic implications of this finding.

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Publication Details

Journal
BMJ Case Reports
Published
2026-02-01
DOI
https://doi.org/10.1136/bcr-2025-267762
Primary Topic
Hereditary Neurological Disorders
Type
article
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article

Novel KIF5A variant in a patient with early-onset levodopa-responsive Parkinson’s syndrome

Magdeldin Elgizouli, Benjamin Tatrai, Maria R Kuzmanova, Boyana R Kuzmanova et al.
BMJ Case Reports
Hereditary Neurological Disorders
article

Novel KIF5A variant in a patient with early-onset levodopa-responsive Parkinson’s syndrome

Magdeldin Elgizouli, Benjamin Tatrai, Maria R Kuzmanova, Boyana R Kuzmanova, J Carsten Möller
article en

Abstract

We present the case of a male in his mid-30s with a progressive complex neurological phenotype primarily characterised by levodopa-responsive parkinsonism with motor fluctuations as well as gait ataxia, peripheral neuropathy and finally also spastic paraplegia. Genetic analysis identified a novel heterozygous variant in the KIF5A gene: c.937G>A (p.Glu313Lys). This variant is genetically classified as likely pathogenic. Other pathogenic mutations in the KIF5A gene are associated with hereditary spastic paraplegia type 10, Charcot-Marie-Tooth disease type 2 and amyotrophic lateral sclerosis. We discuss the clinical, genetic and prognostic implications of this finding.

BMJ Case ReportsVol. 19(2)
University of Zurich (CH), University Hospital of Zurich (CH), Hirslanden Private Hospital Group (CH), Réseau Fribourgeois de Santé Mentale (CH)
Good health and well-being
Openalex Percentile: Top 71%
Hereditary Neurological Disorders
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