GALNS and mucopolysaccharidosis type 4A: Mucopolysaccharidosis type IVA (MPS IVA; Morquio Syndrome [OMIM #253000]) is a rare, incurable, autosomal recessive lysosomal storage disorder (LSD) that is caused by a deficiency of the enzyme N-acetyl-galactosamine-6-sulfatase - GALNS [1, 2].