Glutaric Acidemia is a rare genetic disorder that affects the body's ability to break down certain amino acids, particularly lysine and tryptophan. This condition leads to the accumulation of harmful substances, specifically glutaric acid, in the body, which can cause various health issues, including neurological problems. Symptoms of Glutaric Acidemia may include developmental delays, movement disorders, and seizures. Early diagnosis through newborn screening and prompt treatment can help manage the condition and improve quality of life. Treatment often involves dietary restrictions and supplementation to prevent the buildup of toxic substances.