In Hunter syndrome, lack of the enzyme iduronate sulfate sulfatase leads to buildup of carbohydrates called mucopolysaccharides. In severe cases, this may swell the liver, spleen, and heart. In mild cases, deafness may be the only symptom. A child with this syndrome is deaf and has unusual facial features. Hunter syndrome is X-linked recessive. Intellect is usually unimpaired and life span can be normal. Suppose a man who has mild Hunter syndrome has a child with a carrier. a. What is the probability that a male child would inherit Hunter syndrome? b. What is the chance that a female child would inherit Hunter syndrome? c. What is the chance that a girl would be a carrier? d. How might a carrier of this condition experience symptoms?