Publications by authors named "Jae-Gun Moon"
Infants with Sandhoff disease typically appear normal until 3-6 months of age. As the disease progresses, they present with symptoms such as loss of motor skills, exaggerated startle response to loud noise, seizures, visual loss, and paralysis. We encountered a rare case of a 22-month-old girl with Sandhoff disease characterized by progressive motor weakness and dysphagia, who initially showed signs of aspiration at 20 months of age.
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- The study aimed to identify clinical features that could predict improvements in gait speed following robotic-assisted gait training (RAGT) in patients with motor incomplete spinal cord injuries.
- 29 patients participated in a 4-week RAGT program, and their progress was measured using various assessments before and after treatment.
- Key findings indicated that younger age, shorter disease duration, and better baseline physical functions were associated with improved outcomes, highlighting specific assessment tools that could predict treatment success.