Isolated unilateral medial rectus palsy: a rare presentation of midbrain infarction in a child
DOI:
https://doi.org/10.18203/2349-3291.ijcp20243870Keywords:
Fabry diseases, Isolated medial rectus palsy, Midbrain infarction, DiplopiaAbstract
This case study describes a rare instance of isolated unilateral medial rectus palsy in a young patient with Fabry disease, an X-linked lysosomal storage disease. A five-and-a-half-year-old child did not exhibit any other symptoms associated with a stroke, other than abrupt onset diplopia and a pronounced left-eye squint. Isolated medial rectus palsy as a sole presentation of midbrain infarct is a rare entity. Fabry disease is associated with an increased risk of ischemic strokes in patients because of the build-up of glycosphingolipids in the vascular endothelium. This case emphasizes how crucial it is to conduct early neuroimaging and to have a high index of suspicion when dealing with uncommon neurological presentations, particularly in individuals who have underlying genetic conditions like Fabry disease.
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References
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