Join us for an illuminating webinar sponsored by Takeda, offering a comprehensive overview of Hunter Syndrome (MPS II) – Diagnosis and Management. This insightful session will delve into the intricacies of this rare genetic disorder, covering key aspects of diagnosis, treatment, and patient care. Led by esteemed experts in the field of pediatric genetics and immunology the webinar aims to enhance understanding and awareness surrounding Hunter Syndrome. Gain valuable insights into the latest advancements in diagnosis techniques and management strategies, as well as have the opportunity to engage with leading professionals in the field. 

Overview of 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

Professor & Consultant Geneticist, Department of Paediatrics | Government Medical College, Thiruvananthapuram

Dr. Sankar V Hariharan

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