What is Leigh syndrome and what help is available for families? Leigh Syndrome is a rare, inherited neurometabolic disorder, arising from genetic mutations that impair mitochondrial function. Symptoms can manifest in various ways, including loss of motor skills, seizures, lactic acidosis, and progressive neurological decline. Cure MITO Foundation offers a hub of resources, community support, and research initiatives. It connects families to the latest information, treatment advancements, and a n
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What is Leigh syndrome and what help is available for families? Leigh Syndrome is a rare, inherited neurometabolic disorder, arising from genetic mutations that impair mitochondrial function. Symptoms can manifest in various ways, including loss of motor skills, seizures, lactic acidosis, and progressive neurological decline. Cure MITO Foundation offers a hub of resources, community support, and research initiatives. It connects families to the latest information, treatment advancements, and a n
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