Are you a healthcare professional looking to learn more about Hunter syndrome (mucopolysaccharidosis type II, MPS II), a rare genetic disease? You may be one of the first physicians to come into contact with a child affected by this progressive disease, so being equipped to recognise the key signs and symptoms is crucial to facilitate optimum patient management. 

This eBook provides information on: common presenting complaints and clusters of childhood illnesses which could indicate Hunter syndrome, diagnosis pathway, multidisciplinary patient management and additional learning resources, along with the stories of families affected by Hunter syndrome.

All patient images in this eBook are used with permission, and cannot be copied or reused in any form.

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