Article Text
Rare disease
CASE REPORT
Rare case of Gordon Holmes syndrome
Summary
Young-onset cerebellar syndromes are quite interesting and challenging for treating clinicians. While dealing with such cases, a clinician should be aware of rare possible causes too. We report a rare case of Gordon Holmes syndrome—an autosomal recessive cerebellar ataxia with endocrinal abnormalities.
- neurology (drugs and medicines)
- movement disorders (other than parkinsons)
- neuroendocrinology
- neuroimaging
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Footnotes
Contributors RV made the hypothesis, MM made the draft, CS helped in taking images and SS edited the paper.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient consent Obtained.
Provenance and peer review Not commissioned; externally peer reviewed.