Rare Genetic Disorders Emphasized at Awareness Camp in Jammu

Rare Genetic Disorders Emphasized at Awareness Camp in Jammu

JAMMU, DECEMBER 10: A collaborative effort between the Department of Pediatrics, GMC Jammu and the University of Jammu's Department of Zoology/ Institute of Human Genetics, along with the Department of Science & Technology, marked an awareness camp cum seminar on "Common and Rare Genetic Disorders" at SMGS Hospital in Jammu today.

Commissioner Secretary of Science & Technology, Saurabh Bhagat, was the keynote speaker at the event. He highlighted the collective impact of medical science and non-medical science in medical investigation and treatment of diseases, emphasizing the role of Artificial Intelligence in optimizing diagnosis and treatment plans for rare genetic disorders.

Bhagat pointed out that his department funds numerous research projects in this field. He also emphasized the need for doctors to take initiatives for entrepreneurship and start-ups in medical science.

Dr Ashutosh Gupta, Principal & Dean of Government Medical College, Jammu, was the guest of honour on the occasion. He appreciated the organizers of the event and stressed upon the necessity of establishing a fully functional genetic laboratory within their institution.

Professor Ghanshyam Saini of the Pediatrics Department delivered a lecture on "Common and Rare Genetic Disorders," providing an overview of these disorders and describing the work done by pediatricians in this area.

Associate Professor Dr Swarkar Sharma from the Department of Molecular Biology, Central University Jammu, shared detailed insights into Common and Rare Genetic Disorders, shedding light on their prevalence, affected populations, especially in the region of Jammu & Kashmir.

The event brought together prominent personalities including Dr Ashok Gupta, Former HOD Pediatrics GMC Jammu; Dr Dara Singh, Medical Superintendent SMGS Hospital Jammu; Dr N K Pargal, among others. The seminar is expected to promote awareness and understanding of rare genetic disorders in the region.