Krabbe Disease is a rare genetic disorder that affects the nervous system. It is caused by a deficiency of the enzyme galactocerebrosidase, which is essential for the breakdown of certain fats in the body. This leads to the accumulation of toxic substances in the brain and nervous system, resulting in severe neurological damage. Symptoms of Krabbe Disease typically appear in infancy and may include irritability, muscle stiffness, and developmental delays. As the disease progresses, affected individuals may experience loss of vision, hearing, and motor skills. Early diagnosis and intervention are crucial for managing the condition, although there is currently no cure.