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Community-based Adapted Tango Dancing for Individuals with Parkinson's Disease and Older Adults
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Relapsing encephalopathy with dancing eyes and jerky limbs.
Nor Amelia Mohd Fauzi1, Suhailah Abdullah2, Ai Huey Tan3
1Department of Medicine, Faculty of Medicine, Universiti Teknologi MARA Sungai Buloh Campus, Selangor, Malaysia.
Parkinsonism & Related Disorders
|March 9, 2019
Summary
This case study details relapsing-remitting opsoclonus-myoclonus-ataxia syndrome (OMAS) in Hashimoto's encephalopathy. Early immunotherapy may improve outcomes for this rare neurological condition.
Area of Science:
- Neurology
- Immunology
- Endocrinology
Background:
- Hashimoto's encephalopathy is an autoimmune disorder affecting the thyroid.
- Opsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare neurological disorder characterized by involuntary eye movements, myoclonus, and ataxia.
- The association between Hashimoto's encephalopathy and OMAS is exceptionally rare.
Observation:
- A patient presented with relapsing-remitting OMAS.
- Comprehensive diagnostic evaluation confirmed Hashimoto's encephalopathy as the underlying cause.
- This represents a rare instance of OMAS manifestation in Hashimoto's encephalopathy.
Findings:
- The study documents a unique case of OMAS linked to Hashimoto's encephalopathy.
- Previous literature has reported only one similar case.
- The relapsing-remitting nature of OMAS in this context highlights the complexity of autoimmune neurological disorders.
Implications:
- Recognizing OMAS as a potential manifestation of Hashimoto's encephalopathy is crucial for accurate diagnosis.
- Early initiation of immunotherapy is suggested to improve clinical outcomes for affected patients.
- This case contributes to understanding the spectrum of autoimmune encephalopathies and their neurological sequelae.
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