HS info: Recent Episodes

Shire

Welcome to the 'HS info?' podcast series.

Hunter syndrome, also known as MPS II, is a rare, multisystemic genetic disorder. You could be one of the first physicians to suspect this progressive and life-limiting disease. Listen to interviews with leading experts who share insights on the symptoms, diagnosis, management and prognosis for people living with the condition.

Each patient has a unique presentation, so it is important to consider the whole patient, including clues outside your area of expertise, in order to help achieve early diagnosis.

Visit Huntersyndrome.info for more information and join the rare disease community at Rare2aware.com.

This podcast series was initiated and funded by Shire and is intended for an international healthcare professional audience.

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Podcast Episode

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Podcast Episode

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Improving the quality of life of MPS II patients and their families with an early diagnosis and appropriate management.

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Minimising the risks associated with surgery in MPS II patients

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Managing a Multisystemic Rare Disorder

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Decreasing the diagnostic delay for a rare genetic disease

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Learn more about this rare, genetic disease

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Learn more about this rare, genetic disease

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ENTs are among the most likely physicians to recognise the early signs and symptoms of Hunter syndrome.

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Professor Joseph Muenzer, Hartmann Wellhoefer MD and Professor Chris Hendriksz discuss the challenges facing rare disease diagnosis and the diagnostic odyssey that rare disease patients often undertake.

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Professor Joseph Muenzer, an expert in MPS diseases, introduces the basics of MPS diseases. This podcast was initiated and funded by Shire and has been developed for an international HCP audience.