Hunter Syndrome
Hunter syndrome is a rare genetic disease that primarily affects boys. Also known as mucopolysaccharidosis II (MPS II), it may be hard to diagnose because many of the signs and symptoms are common childhood complaints.[1]
Visit Huntersyndrome.info for more information.
This channel is a resource created by Takeda that aims to educate about, and increase awareness of, MPS II. It is intended for an international audience outside of the USA. Information on this channel is not intended to diagnose or advise in the treatment of any illness or disease. It is not intended to substitute for consultation with a healthcare provider. Please consult your healthcare provider for professional medical advice.
C-ANPROM/INT//7012 January 2020
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1. Burton BK, Giugliani R. Eur J Pediatr 2012; 171(4)
Dr Florian Lagler: a paediatrician’s advice for families with MPS II
Dr Florian Lagler: a paediatrician and pharmacologist’s experience with MPS II
Professor Maurizio Scarpa: working with families affected by MPS II
Professor Maurizio Scarpa: a metabolic paediatrician’s experience with MPS II
Hunting Hunter syndrome: a rare disease hidden among childhood complaints
The Yin and Yang of Diagnosing MPS II: Suspecting and Testing presented by Professor Giugliani
Hunter Syndrome (MPS II): an uncommon combination of childhood complaints
Dr Christina Lampe, a specialist’s advice for families with MPSII
Dr Christina Lampe: A career in MPS diagnosis and management
MPS II: Family Matters, presented by Dr Christina Lampe
Aiden and Aj's story - living with Hunter syndrome
Hunter, Kingston and Nash’s story – living with Hunter syndrome
Professor Umut Akyol: an ENT specialist’s perspective on MPS II
How Hunter syndrome (MPS II) progresses
Professor Umut Akyol: an ENT specialist’s perspective on the diagnosis and management of MPS II
Differential diagnoses of MPS II, presented by Professor Umut Akyol
Simulation of a perioperative (ENT) complication in a Hunter patient, presented by Dr Florian Lagler
An Introduction to the MPS Family, presented by Professor Roberto Giugliani
A Rare Specialism: a look at the last ten years in MPS management, presented by Dr Christina Lampe
Christina Lampe, Familial Connections
Bob Stevens, My Experience with MPS II
Complications in Hunter Syndrome, presented by Dr Florian Lagler
Are you missing Hunter Syndrome? Presented by Professor Umut Akyol
Bob Stevens, MPS II and the MPS Society
My most memorable MPS II diagnosis, Anna Tylki-Szymanska
Professor Anna Tylki-Szymanska, 30 years in MPS
My career in MPS (mucopolysaccharidosis) – with Professor Roberto Giugliani
My career in MPS (mucopolysaccharidosis) – with Professor Maurizio Scarpa
My career in MPS (mucopolysaccharidosis) – with Dr Christina Lampe
Living with Hunter syndrome (MPS II) - The Balancing Act (Part 2)