Hunter Syndrome (MPS II) Information

Hunter syndrome (Mucopolysaccharidosis II, MPS II) is a serious progressive genetic disorder that affects boys almost exclusively. It is caused by a deficiency or absence of the lysosomal enzyme iduronate-2-sulfatase (I2S). This enzyme is required for the degradation of specific glycosaminoglycans (GAG); thus its absence results in a harmful accumulation of these substances in cells throughout the body.

OnePath^SM Services for Hunter Syndrome

OnePath^SM is the support center that can help you, your staff, and your patients with many aspects of therapy.

• Provide streamlined support through a case manager dedicated to assisting you and your patient with many aspects of therapy
• Help your staff by providing information on coding, reimbursement, and insurance verification
• Provide assistance with prior authorization, such as sample letters of medical necessity
• Assists in identifying potential treatment sites, if necessary
• Assist with treatment compliance by following up with patients and their families about their appointments