Join us for an insightful webinar that delves into two critical lysosomal storage disorders: Hunter Syndrome (MPS II) and Gaucher Disease (GD). This session is tailored for healthcare professionals aiming to enhance their understanding of the diagnosis and management of these rare but significant conditions. The discussions will be led by distinguished experts who bring both clinical and academic expertise to the table.
The first topic, Hunter Syndrome (MPS II): Diagnosis and Management, will be presented by Dr. Barnali Das, Assistant Professor of Paediatrics at the Institute of Child Health, Kolkata. This session will explore the clinical features of MPS II, the challenges in achieving early diagnosis, and current therapeutic options. Dr. Das will provide practical insights into identifying and managing this rare genetic disorder effectively.
The second topic, Gaucher Disease (GD): Diagnosis and Management, with Dr. Radha Rama Devi, Senior Consultant at Rainbow Children’s Hospital and Sandor Life Sciences, Hyderabad, as the speaker. Dr. Devi will focus on the diagnostic approaches and treatment strategies for GD, highlighting recent advancements in therapy and their implications for patient care.

Overview of Hunter Syndrome & Overview of Gaucher Disease- Diagnosis & Management

Takeda brings to you a journey into the realm of MPS II with our distinguished panel of medical experts. Our esteemed doctors will offer a thorough overview of the condition, covering its diagnosis, treatment options, and recent advancements in the field. Following the insightful presentations, engage in a stimulating panel discussion where our experts will address key questions and explore emerging trends in MPS II management. 
Don't miss this exclusive opportunity to enhance your understanding of MPS II and connect with peers in the medical community. Register now to secure your spot in this engaging webinar.

Overview on Hunter Syndrome (MPS II) – Diagnosis and Management

An hereditary condition of carbohydrate metabolism called mucopolysaccharidosis II (MPS II) nearly exclusively affects men. It is distinguished by unusual facial features, a large head, hydrocephalus, hepatosplenomegaly, an umbilical or inguinal hernia, and hearing loss. Individuals with MPS II experience symptoms that range widely in severity. Join us for this fascinating discussion about the signs, causes, and treatment of MPS-II, hosted by Takeda, featuring eminent medical professionals like Dr. Sankar V H, Additional Professor & Consultant Geneticist, Department of Paediatrics, Government Medical College, Thiruvananthapuram, Dr. Kausik Mandal, Additional Professor, Department of Medical Genetics, Sanjay Gandhi Post-Graduate Institute of Medical Sciences, and Dr. Akella Radha Rama Devi, Consultant, Rainbow Children Hospital, Hyderabad.

Early Diagnosis & Management of MPS II - A Case Based Approach

Consultant | Rainbow Children Hospital, Hyderabad.

Dr. Akella Radha Rama Devi

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