Profile Details
Dr. Mamta Muranjan
Professor – Pediatrics & In-Charge, Genetic Clinic and Pediatric Genetics Research Laboratory
Seth G.S. Medical College & KEM Hospital, Mumbai, India.
Dr. Mamta Muranjan is a respected pediatrician, clinical geneticist, and academic leader serving as Professor of Pediatrics and Head of the Pediatric & Genetics Research Laboratory (Genetic Clinic) at Seth G.S. Medical College & King Edward Memorial (KEM) Hospital, Mumbai, one of India’s oldest and most renowned pediatric centers. In this capacity, she oversees clinical, diagnostic, and research activities in pediatric genetics and metabolic disorders, guiding one of the country’s most established laboratory programs that investigates and manages genetic and inborn errors of metabolism in children while also mentoring future generations of clinicians and scientists.
Dr. Muranjan’s leadership at the Genetic Clinic is built on a strong foundation in pediatric medicine and genetics—having completed her MBBS, MD (Pediatrics), and Diploma in Child Health—and reflects decades of dedicated work in clinical genetics, newborn screening, prenatal diagnosis, and the care of children with congenital and hereditary disorders. Under her stewardship, the clinic has continued to deliver high-quality diagnostic services to patients referred from across India, integrating laboratory expertise with compassionate patient-centered care.
Throughout her career, Dr. Muranjan has contributed substantially to both clinical practice and scientific knowledge. Her publications include research on Takayasu’s arteritis, organic acidemias, Down syndrome, and other complex pediatric conditions, evidencing her engagement in advancing understanding of rare and inherited disorders in Indian children. She has also played a pivotal role in academic and continuing medical education, organizing genetics workshops and contributing to postgraduate teaching and training programs at KEM.
Beyond clinical service and research, she has taken on broader roles in rare disease leadership and policy, including serving as a nodal officer for rare diseases at KEM’s Centre of Excellence and participating in national expert groups on rare disorders and genetic diagnostics—reinforcing her impact on both institutional and national efforts to enhance genetic healthcare capacity.
Dr Muranjan’s career exemplifies a rare blend of deep clinical expertise, research acumen and academic mentorship, positioning her as a pivotal figure in pediatric genetics in India and a trusted leader in advancing care for children with complex genetic and metabolic conditions
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