Leigh Syndrome
Leigh Syndrome is a rare genetic disorder that affects the brain and nervous system, typically appearing in infants and young children. It is characterized by progressive neurological deterioration, often leading to motor skills loss, breathing difficulties, and severe developmental delays. The condition is linked to issues with energy production in cells, usually due to mitochondrial dysfunction—problems in the powerhouses of cells. Symptoms can vary widely, and while there is no cure, supportive treatments can help manage symptoms. Life expectancy varies, with some children surviving into adolescence or adulthood, but many have a shortened lifespan.
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Leigh syndrome is a rare genetic disorder that affects the central nervous system, particularly the brain. It typically arises in early childhood and leads to progressive neurological deterioration. Symptoms can include developmental delays, muscle weakness, difficulty with movement, seizures, and problems with breathing and heart function. The condition is caused by mutations in genes involved in energy production within cells, which leads to dysfunction in brain cells. While there is no cure, supportive treatments can help manage symptoms and improve quality of life for affected individuals.