A 12-Month-Old Female Infant Exhibits Severe Developmental Delay with Associated

A 12-month-old female infant exhibits severe developmental delay with associated macrocephaly, dysmorphic facies, hypotonia, and hepatosplenomegaly. Clouding of the corneas is not evident. A pebbly ivory-colored lesion is present over the infant's back. The activity of iduronate sulfatase in the plasma is not detectable. These symptoms are indicative of which type of mucopolysaccharidosis?

A) Ehlers-Danlos syndrome
B) Hunter syndrome
C) Hurler syndrome
D) Marfan syndrome
E) osteogenesis imperfecta