Mucopolysaccharidosis type 4B

A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme beta galactosidase. It is characterized by skeletal dysplasia and short stature.

Also known as: Beta-D-galactosidase deficiency, MPS 4B, MPS IV B, MPS4B, MPSIVB, Morquio disease type B, Morquio syndrome B, mucopolysaccharidosis type IVB

67 clinical trials for this condition and its sub-types.