Evidence map›Paper›PMID 41394932›Full record

ArticleClinical case reports2025

A Diagnosis Hidden in Plain Sight: A Rare Presentation of Isolated Dysarthria in Wilson's Disease-A Case Report.

Kruthika Reddy, Maanini Singhvi, Archana B Netto, B Thejus, Leroy D Souza, Deepak B Shivananda, Samyuktha Vinu Nair, Deepak Rai

Abstract read
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Article in Clinical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Kruthika ReddyBangalore Medical College and Research Institute Bangalore India.ORCID https://orcid.org/0009-0004-5308-3601
Maanini SinghviBangalore Medical College and Research Institute Bangalore India.ORCID https://orcid.org/0000-0001-9292-9535
Archana B NettoBangalore Medical College and Research Institute Bangalore India.ORCID https://orcid.org/0000-0001-9897-0299
B ThejusBangalore Medical College and Research Institute Bangalore India.ORCID https://orcid.org/0000-0002-9067-9402
Leroy D SouzaBangalore Medical College and Research Institute Bangalore India.ORCID https://orcid.org/0009-0006-8031-2822
Deepak B ShivanandaBangalore Medical College and Research Institute Bangalore India.ORCID https://orcid.org/0009-0009-3601-3886
Samyuktha Vinu NairBangalore Medical College and Research Institute Bangalore India.ORCID https://orcid.org/0009-0006-1014-371X
Deepak RaiAmppipal Hospital Gorkha Nepal.ORCID https://orcid.org/0009-0006-3766-3096

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A clinical picture of isolated dysarthria is relatively uncommon, and the underlying condition causing it can be easily misdiagnosed. In this case, a 24-year-old Indian male presented with complaints of slurring of speech occurring for the past 9 months. The patient also complained of difficulty swallowing food using his tongue. There was also a history of excessive drooling of saliva. There was no history of involuntary movements suggestive of tremor, limb dystonia, Parkinsonism, ataxia, behavioral abnormalities, or any significant cognitive impairment. The patient's parents had a non-consanguineous marriage, and there were no similar complaints among the patient's siblings. The patient was started on copper chelating agents and speech therapy and noticed remarkable improvement as per his own account. Clinical examination showed Kayser-Fleischer rings in the eyes, raised serum ceruloplasmin, and significant MRI findings. If symptoms like isolated dysarthria are encountered, a thorough work-up must be done to rule out any underlying neurological problems. The key teaching point revolves around the consanguinity of marriages in India should raise an index of suspicion for autosomal recessive conditions and movement disorders.

Indexed as

consanguinityD‐penicillaminedysarthriaKF ringsneuropsychiatric symptomsWilson's disease

Identifiers

PMID41394932
PMCPMC12695676

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.