This research aims to clarify the necessity of ruling out other possible causes for spinal cord lesions in individuals carrying the m.3243A>G mutation.
Examined cases of spinal cord lesions in individuals with the m.3243A>G mutation
Emphasized the process of differential diagnosis to ensure accurate attribution to mitochondrial disease
Identified significant variation in spinal cord lesion presentations among carriers
Recommended comprehensive evaluation to prevent misdiagnosis of mitochondrial disease in m.3243A>G carriers