Mucopolysaccharidosis type II : Hunter's syndrome

Publication Date

2013

Document Type

Research

Abstract

This is a case of 5 years old male, with impaired communication, social interaction and play pattern, with associated facial dysmorphism, thus diagnosed with Hunter Syndrome, autism spectrum disorder. The management of the clinical problems seem supportive, it is typically complex and requires the medical expert to be aware of the special issues surrounding the patient, and a multidisciplinary approach must be helpful. The challenges for parent, families and caregivers with children possessing severe disabilities are great. Intense supervision needed for the child can cause families to become physically, mentally and emotionally exhausted.

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