Evidence map›Paper›PMID 41414999›Full record

ArticleFrontiers in neurology2025

Clinical phenotypes of motor neurone disease in a Kenyan hospital-based population.

Effie Nailah Kamadi, Jasmit Shah, Juzar Hooker, Thomas M Jenkins, Dilraj Singh Sokhi

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Article in Frontiers in neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Effie Nailah KamadiDepartment of Medicine, Aga Khan University Medical College of East Africa (Nairobi Campus), Nairobi, Kenya.
Jasmit ShahDepartment of Medicine, Aga Khan University Medical College of East Africa (Nairobi Campus), Nairobi, Kenya.
Juzar HookerDepartment of Medicine, Aga Khan University Medical College of East Africa (Nairobi Campus), Nairobi, Kenya.
Thomas M JenkinsCurtin University, Medical School (Perth Campus), Perth, WA, Australia.
Dilraj Singh SokhiDepartment of Medicine, Aga Khan University Medical College of East Africa (Nairobi Campus), Nairobi, Kenya.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Motor neurone disease (MND) presentation is globally heterogenous and data on the clinical phenotype in Sub-Saharan Africa (SSA) is scarce. We sought to address this by describing the profile of MND patients in a Kenyan hospital-based population. Methods: The medical charts of all adult MND patients assessed in the facility between January 2010 and December 2023 were retrospectively reviewed. The biographical data and clinical features of these patients were captured from their electronic and manual health records and statistical analysis performed. Results: In total, 160 patients had their data analyzed. The male to female ratio was 1.76:1. The median age at presentation was 55.0 (IQR: 45.0-68.0) years with a median diagnosis delay of 4.0 (IQR: 2.0-8.5) months. The site of first symptom onset was the lower limbs in 34.4% and the bulbar region in 33.1% [ Conclusion: This Kenyan case series of MND patients demonstrated a higher rate of bulbar onset disease [

Indexed as

amyotrophic lateral sclerosisclinical phenotypeHIVhospital-based studymotor neurone diseaseneurodegenerative disordersSub-Saharan Africa/Kenya

Identifiers

PMID41414999
PMCPMC12710236

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