Evidence map›Paper›PMID 39649858›Full record

ArticleAnnals of medicine and surgery (2012)2024

Clinical diagnosis and management of spinocerebellar ataxia in a resource-constrained setting: a case report from Eastern Nepal.

Nabin Adhikari, Popular Pokhrel, Priyanka Kc, Navin Kumar Sah, Bhupendra Shah

Abstract readCase Reports
In one paragraph

Article in Annals of medicine and surgery (2012), 2024. 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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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Nabin AdhikariB.P. Koirala Institute of Health Sciences, Dharan, Nepal.ORCID https://orcid.org/0009-0000-4926-2384
Popular PokhrelB.P. Koirala Institute of Health Sciences, Dharan, Nepal.ORCID https://orcid.org/0009-0004-4209-7004
Priyanka KcDepartment of Internal Medicine, B.P. Koirala Institute of Health Sciences, Dharan, Nepal.ORCID https://orcid.org/0009-0002-2720-3310
Navin Kumar SahDepartment of Internal Medicine, B.P. Koirala Institute of Health Sciences, Dharan, Nepal.
Bhupendra ShahDepartment of Internal Medicine, B.P. Koirala Institute of Health Sciences, Dharan, Nepal.ORCID https://orcid.org/0000-0003-4370-0464

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Spinocerebellar ataxias (SCA) are a diverse group of neurodegenerative disorders with autosomal dominant inheritance, primarily affecting the cerebellum and its connections. Diagnosis typically involves genetic testing, but in resource-limited settings, clinical and neuroimaging assessments become critical. This case report highlights the role of nongenetic methods in diagnosing SCA and outlines management strategies in such settings. Case Presentation: A 41-year-old male presented with a 2-year history of progressive gait imbalance, headache, and abnormal speech. He had a family history of similar symptoms in two siblings, but no significant past medical history. Clinical examination revealed scanning speech, dysmetria, and a broad-based gait. Clinical and neuroimaging findings, including cerebellar atrophy, led to a diagnosis of SCA in the absence of genetic testing. Patient management with speech, occupational, and physical therapies, showed gradual improvement. Discussion: SCA, characterized by cerebellar atrophy and a range of clinical symptoms, is typically diagnosed through genetic testing, but clinical and imaging assessments are crucial when genetic resources are limited. This case illustrates that a comprehensive clinical evaluation, including neuroimaging, can support the diagnosis of SCA even without genetic testing. Strategic management emphasizing symptomatic relief and functional improvement through a multidisciplinary approach, including regular follow-up and personalized therapy, are crucial, as evidenced by the timely improvement observed in our case. Conclusion: In resource-limited settings, a comprehensive clinical and neuroimaging assessment is essential for diagnosing spinocerebellar ataxia when genetic testing is not feasible. Effective management through multidisciplinary therapies can improve patient outcomes, underscoring the need for innovative strategies to enhance diagnostic and treatment capabilities in such environments.

Indexed as

case reportresource-limited settingspinocerebellar ataxia

Identifiers

PMID39649858
PMCPMC11623831

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