Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Lysosomal storage disease with skeletal involvement · Mucopolysaccharidosis type 3
Mucopolysaccharidosis type 3B
A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme N-acetyl-alpha-D-glucosaminidase. It is characterized by behavioral changes, sleep disturbances, and mental developmental delays.
This condition has no sub-types.