ABOUT THE WEBINAR

Mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome, is a condition that affects many different parts of the body and occurs almost exclusively in males. It is a progressively debilitating disorder; however, the rate of progression varies among affected individuals. ERT offers conservative management with evidence based favourable survival outcomes.

HUNTER SYNDROME

Early screening & management

Acquire knowledge of a very rare, progressive MPS II disorder screening and management.

18th SEPTEMBER, 2020

ONLINE | 4 - 5 PM IST 

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THE SPEAKER

Dr. Sankar V. Hariharan

  • Dr. Sankar V. Hariharan has done his MBBS, MD (Paediatrics) from Government Medical College, Thiruvananthapuram and DM from Sanjay Gandhi Postgraduate Institute of Medical Sciences.

  • Presently working as Additional professor & Geneticist in Department of paediatrics at Government Medical College, Thiruvananthapuram, Kerala. 

  • Dr. Hariharan has an experience of over 23 years post PG teaching of undergraduates and postgraduates in Paediatrics and 13 years in Medical Genetics. 

  • He has been the principal investigator in multiple projects including a multi centric study on Clinical, Biochemical and Molecular characterization of Lysosomal storage disorders (ICMR study).

  • He has more than 30 publications in national and international journals and around chapters in 10 textbooks. He is a reviewer of six indexed national/international journals. He is a founder member of Indian Academy of Medical genetics (IAMG).

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Expert faculty

Q&A session

In-depth guidelines

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DID YOU KNOW?

Hunter syndrome is almost always diagnosed in males. Doctors diagnose it in roughly 1 out of 100,000 to 170,000 males.

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WHO IS IT FOR?

Geneticists

Orthopaedic Doctors

Paediatrics

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Internal Medicine

MBBS, MD (Paediatrics), DM (Medical Genetics)

This information is solely intended for the use of Registered Medical Practitioner only. The information contained herein is based on the published medical literature and international recommended guidelines. The information provided is intended for educational purposes only, aimed at increasing awareness on Hunter Syndrome and not meant for promotion of any specific product. Takeda makes no representation or warranty concerning the information / content provided, and assumes no responsibility for the accuracy of the opinion furnished or any outcome based on the application of such information. 

“TAKEDA and the TAKEDA logo are trademarks or registered trademarks of Takeda Pharmaceutical Company Limited”.

This material contains copyright protected information, content; the use of which is limited by law and this material cannot be reproduced, replicated, used or modified by any person for their own use or further distribution.

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Webinar brought to you by

Opening remarks by Dr. Parikshit 

(16:00 - 16:05)

Keynote session by Dr. Sankar on Hunter Syndrome (16:05 - 16:45)

Questions & Answers with Dr. Sankar

(16:45 - 16:55)