Thalassemias are the most common single genetic disorders known till date. It is characterized by the deficient synthesis of one or more of the globin polypeptide chains that result in an imbalance between the numbers of alpha and beta globin chains. The end result is ineffective erythropoiesis, hypochromic RBCs, microcytosis, and hemolysis which consequently lead to anemia. In this session, renowned Clinical Genticist, Dr. Chaitanya will provide a full guide for the Evaluation and Management of Thalassaemia.

Clinician's Approach To Thalassaemia

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

Clinical & Metabolic Geneticist and In-Charge of Clinical Genetics Unit, Bharati Vidyapeeth Hospital, Medical College and Research Centre, Pune

Dr. Chaitanya Ashok Datar

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