Professor Maurizio Scarpa: working with families affected by MPS II
Professor Maurizio Scarpa is a world-leading expert on Hunter syndrome (mucopolysaccharidosis type II, MPS II), having been involved in the research and management of this rare disease, as a paediatrician since 1986.
In this video, Professor Scarpa explains what Hunter syndrome is, and how it impacts families before and after a diagnosis.
Children with Hunter syndrome often don’t show any signs of the condition at birth, however, as they get older they can experience a combination of childhood complaints, including regular ear infections and hernias. They may also be affected by developmental delays.
An uncommon combination of common childhood complaints may raise suspicion of Hunter syndrome. If you have any concerns, please speak to your physician about Hunter syndrome.
For more information on Hunter syndrome, please visit http://www.huntersyndrome.info/
The resources mentioned and information found on this channel are not exhaustive, and are not intended to diagnose or advise about the treatment of any illness or disease. This information should not be used in place of advice from your general practitioner or other healthcare professional. If in doubt, please contact your doctor for advice.
To learn more from MPS II experts, and hear first-hand what life is like for families living with this rare disease, visit our channel at: https://www.youtube.com/user/HunterSy...
You can also find more information by referring to your local MPS society and the European Organisation for Rare Diseases.
C-ANPROM/INT/HUNS/0107 February 2021
Takeda Pharmaceutical Company Limited. All rights reserved.
Видео Professor Maurizio Scarpa: working with families affected by MPS II канала Hunter Syndrome
In this video, Professor Scarpa explains what Hunter syndrome is, and how it impacts families before and after a diagnosis.
Children with Hunter syndrome often don’t show any signs of the condition at birth, however, as they get older they can experience a combination of childhood complaints, including regular ear infections and hernias. They may also be affected by developmental delays.
An uncommon combination of common childhood complaints may raise suspicion of Hunter syndrome. If you have any concerns, please speak to your physician about Hunter syndrome.
For more information on Hunter syndrome, please visit http://www.huntersyndrome.info/
The resources mentioned and information found on this channel are not exhaustive, and are not intended to diagnose or advise about the treatment of any illness or disease. This information should not be used in place of advice from your general practitioner or other healthcare professional. If in doubt, please contact your doctor for advice.
To learn more from MPS II experts, and hear first-hand what life is like for families living with this rare disease, visit our channel at: https://www.youtube.com/user/HunterSy...
You can also find more information by referring to your local MPS society and the European Organisation for Rare Diseases.
C-ANPROM/INT/HUNS/0107 February 2021
Takeda Pharmaceutical Company Limited. All rights reserved.
Видео Professor Maurizio Scarpa: working with families affected by MPS II канала Hunter Syndrome
Показать
Комментарии отсутствуют
Информация о видео
Другие видео канала
![Differential diagnoses of MPS II, presented by Professor Umut Akyol](https://i.ytimg.com/vi/DfybzPXvbAw/default.jpg)
![Awareness and diagnosis of Hunter syndrome (MPS II)](https://i.ytimg.com/vi/Jkq4LzH0QfQ/default.jpg)
![Surgery and otorhinolaryngology: MDT management of Hunter syndrome (MPS II)](https://i.ytimg.com/vi/uQS_hmTfPd4/default.jpg)
![Anaesthesia: MDT management of Hunter syndrome (MPS II)](https://i.ytimg.com/vi/ZGIikLNh1IM/default.jpg)
![The role of surgeons in early diagnosis of Hunter syndrome (MPS II)](https://i.ytimg.com/vi/bKCmPBF7VHM/default.jpg)
![My most memorable MPS II diagnosis, Anna Tylki-Szymanska](https://i.ytimg.com/vi/LZVRsgbNp6U/default.jpg)
![Christina Lampe, Familial Connections](https://i.ytimg.com/vi/R-iXRzwxj2A/default.jpg)
![An Introduction to the MPS Family, presented by Professor Roberto Giugliani](https://i.ytimg.com/vi/ZGgL9ThjRkU/default.jpg)
![My career in MPS (mucopolysaccharidosis) – with Dr Christina Lampe](https://i.ytimg.com/vi/zTbvNIwUJ50/default.jpg)
![Signs and symptoms of Hunter syndrome (MPS II) - The Balancing Act (Part 1)](https://i.ytimg.com/vi/0vi2FncDF5w/default.jpg)
![Simulation of a perioperative (ENT) complication in a Hunter patient, presented by Dr Florian Lagler](https://i.ytimg.com/vi/ZsHfS7Olcf4/default.jpg)
![Bob Stevens, My Experience with MPS II](https://i.ytimg.com/vi/WEc-SnUqOtI/default.jpg)
![Professor Maurizio Scarpa: a metabolic paediatrician’s experience with MPS II](https://i.ytimg.com/vi/ymUXCvdO8P0/default.jpg)
![Elsa Shapiro Measuring Cognition in MPS II](https://i.ytimg.com/vi/QsNnlAVZZ0s/default.jpg)
![Professor Umut Akyol: an ENT specialist’s perspective on the diagnosis and management of MPS II](https://i.ytimg.com/vi/3H_rRP2A0UI/default.jpg)
![Hunting Hunter syndrome: a rare disease hidden among childhood complaints](https://i.ytimg.com/vi/QJYy4wbVcJk/default.jpg)
![Living with Hunter syndrome (MPS II) - The Balancing Act (Part 2)](https://i.ytimg.com/vi/KlkI5697IIg/default.jpg)
![Professor Umut Akyol: an ENT specialist’s perspective on MPS II](https://i.ytimg.com/vi/RYJP38wQ1oc/default.jpg)
![My career in MPS (mucopolysaccharidosis) – with Professor Roberto Giugliani](https://i.ytimg.com/vi/vjGyEI1OQcc/default.jpg)
![Hunter Syndrome (MPS II): an uncommon combination of childhood complaints](https://i.ytimg.com/vi/7kBGEYAFhJw/default.jpg)