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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