Hunter syndrome is a rare genetic disease. An enzyme needed by your body cannot be produced. It appears in children as young as 2 years old. It almost always occurs in males. Initial symptoms include abdominal hernia, ear infections, and symptoms of common cold. Patient may also have a big head and big abdomen. It will eventually lead to permanent physical and mental damages. Hunter syndrome is very difficult to treat. The most effective treatment is bone marrow transplant.
How is Hunter syndrome treated in practice?