Diseases and Conditions
Hunter syndrome
Overview
Symptoms
Causes
Risk factors
Complications
Prevention
Diagnosis
Treatment
Coping and support
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Causes
Hunter syndrome develops when a defective chromosome is inherited from the child's mother.
Because of that defective chromosome, an enzyme that's needed to break down complex sugar molecules is missing or malfunctioning. Without this enzyme, massive amounts of these complex sugar molecules collect in the cells, blood and connective tissues, causing permanent and progressive damage.