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Adie's pupil and systemic manifestations: a rare unilateral presentation
M N Vimisha1, M Shah Virna1, Kumar Karthik1
1Department of Neuro-Ophthalmology, Aravind Eye Hospital and Postgraduate Institute, Coimbatore, India.
GMS Ophthalmology Cases
|January 15, 2025
Summary
This case study describes a young woman diagnosed with Holmes-Adie syndrome, a rare neurological disorder. The condition caused vision problems and other neurological signs, highlighting the importance of comprehensive evaluation.
Area of Science:
- Ophthalmology
- Neurology
- Endocrinology
Background:
- Presents a rare case of Holmes-Adie syndrome in a young woman.
- Highlights the diverse and sometimes subtle clinical manifestations of the syndrome.
Observation:
- Patient experienced blurred vision, particularly with near work.
- Ophthalmic and neurological exams revealed light-near dissociation, vermiform iris movements, and absent deep tendon reflexes.
- Laboratory tests showed mild iron deficiency anemia and low vitamin D3 levels.
Findings:
- Orthopedic evaluation revealed right knee arthritis and patellar chondromalacia.
- Pelvic and lumbar MRI identified an ovarian cyst, periurethral cyst, and sacral hemangioma.
- Diagnosis of Holmes-Adie syndrome was confirmed.
Implications:
- This case underscores the importance of a multidisciplinary approach in diagnosing complex neurological conditions.
- Suggests potential links or co-occurrences between Holmes-Adie syndrome and other seemingly unrelated conditions.
- Emphasizes the role of photochromatic lenses in managing visual symptoms associated with Holmes-Adie syndrome.
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