Mucopolysaccharidosis with excessive CHONDROITIN SULFATE B in urine, characterized by dwarfism and deafness. It is caused by a deficiency of N-ACETYLGALACTOSAMINE-4-SULFATASE (arylsulfatase B).
Also Known As:
Syndrome, Maroteaux-Lamy; ARSB Deficiency; Arylsulfatase B Deficiency; Mucopolysaccharidosis 6; Mucopolysaccharidosis Type 6; Mucopolysaccharidosis Type VI; N-Acetylgalactosamine-4-Sulfatase Deficiency; ARSB Deficiencies; Arylsulfatase B Deficiencies; Deficiencies, ARSB; Deficiencies, Arylsulfatase B; Deficiencies, N-Acetylgalactosamine-4-Sulfatase; Deficiency, ARSB; Deficiency, Arylsulfatase B; Deficiency, N-Acetylgalactosamine-4-Sulfatase; Dwarfism, Polydystrophic; Maroteaux Lamy Syndrome; N-Acetylgalactosamine-4-Sulfatase Deficiencies; Type 6, Mucopolysaccharidosis; Type VI, Mucopolysaccharidosis; Maroteaux-Lamy Syndrome; Polydystrophic Dwarfism