Case report highlights diagnostic challenges and neurological decline in a child with saccadic eye movement defects.
Gaucher disease type 3 (GD3) is a rare disorder causing neurological decline, including saccadic eye movement defects. A 2‐year‐old boy, initially treated for anemia, later developed gaze slowness, highlighting the need for careful assessment in children with eye movement issues. Early diagnosis and management are crucial despite costly treatment.
No takes yet. Share an insight, caveat, or question.
Khadayat et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: