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Rare case of Gordon Holmes syndrome
Rajesh Verma1, Mannan Mehta2, Chetan Shettigar2
1Neurology, King George,s Medical University, Lucknow, Uttar Pradesh, India.
Gordon Holmes syndrome, a rare autosomal recessive cerebellar ataxia with endocrine issues, presents a diagnostic challenge in young-onset cases. Awareness of such rare causes is crucial for effective clinical management.
Area of Science:
- Neurology
- Genetics
- Endocrinology
Background:
- Young-onset cerebellar syndromes pose significant clinical challenges.
- Identifying rare etiologies is critical for accurate diagnosis and treatment.
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