Zellweger Syndrome
Description
Zellweger syndrome is a rare, genetic disorder that affects the functioning of peroxisomes, which are responsible for various metabolic processes in the body. This disorder leads to a wide range of symptoms, including developmental delay, liver dysfunction, visual and hearing problems, and abnormal facial features. Zellweger syndrome is usually diagnosed in infancy, and affected individuals often have a significantly reduced life expectancy, with most dying in early childhood. There is no cure, and treatment focuses on managing symptoms and providing supportive care.