Diseases and Conditions
Hunter syndrome
Overview
Symptoms
Causes
Risk factors
Complications
Prevention
Diagnosis
Treatment
Coping and support
Preparing for an appointment
Risk factors
There are two major risk factors for developing Hunter syndrome:
- Family history. Hunter syndrome is caused by a defective chromosome, and a child must inherit the defective chromosome to develop the disease. Hunter syndrome is what's known as an X-linked recessive disease, which means that women carry the defective disease-causing X chromosome and can pass it on. But mothers aren't affected by the disease themselves and likely don't know that they have this defective chromosome.
- Sex. Hunter syndrome nearly always occurs in males. Girls are far less at risk of developing this disease because they inherit two X chromosomes. If one of the X chromosomes is defective, their normal X chromosome can provide a functioning gene. If the X chromosome of a male is defective, however, there isn't another normal X chromosome to compensate for the problem.