Smith-Lemli-Opitz Syndrome

New insights into genetic profiles of movement disorders linked to mitochondrial diseases

Movement disorders (MDs) associated with mitochondrial cytopathies (MCs) exhibit a broad and complex range of symptoms, making diagnosis challenging, according to a poster presented at the 2024 International Congress of Parkinson’s Disease and Movement. Early onset and specific brain MRI findings are key predictors for identifying genetic mutations, though genetic...