Mucopolysaccharidosis I (MPS I)/ HURLER Syndrome
Mucopolysaccharidoses, a group of lysosomal storage diseases, are classified into 11 types according to the genes involved. Type I is the most severe one.
Mucopolysaccharidoses, a group of lysosomal storage diseases, are classified into 11 types according to the genes involved. Type I is the most severe one.
Classic galactosemia is a rare autosomal recessive disorders that causes an inability to digest galactose, which is a breakdown product of lactose. Lactose is found mainly in milk and dairy products.