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Dr. Mamta Muranjan [MBBS, MD, DCH]
🌍 International Patient Helpdesk
+91-8860606766 | +91-9910655125About Dr. Mamta Muranjan [MBBS, MD, DCH]
Dr. Mamta Muranjan is Clinical Geneticist and Currently Working as Consultant - Clinical Genetics in the Clinical Genetics Department at P. D. Hinduja Hospital, Mahim, Mumbai, India.
She is having more than 30 years of experience in the field of paediatrics and clinical genetics.
She has completed her MBBS from the University of Bombay in 1989, DCH from the College of Physicians and Surgeons in 1993 and MD in Paediatrics from the University of Bombay in 1994.
Profile Highlights :
- Dr. Muranjan has 16 years of dedicated experience in clinical genetics. Before this she spent six years as Lecturer and ten years as Associate Professor of Paediatrics at Seth GS Medical College and KEM Hospital, Mumbai, where she combined clinical care of children with teaching and research.
- Her areas of expertise include inborn errors of metabolism, newborn screening, prenatal diagnosis, genetic bone disease, congenital malformations and chromosomal anomalies. Inborn errors of metabolism are inherited conditions in which the body cannot properly process certain nutrients, and early diagnosis through newborn screening can allow treatment before lasting damage occurs.
- She has led significant research, serving as Principal Investigator of the ICMR task force multicentric study on newborn screening for congenital hypothyroidism and congenital adrenal hyperplasia, and of an international phase 3 trial in Gaucher disease type 1. She was earlier a research scientist on the Department of Atomic Energy multicentric study of malformations and Down syndrome in India.
- Dr. Muranjan has published extensively in journals such as Indian Pediatrics, American Journal of Medical Genetics, Archives of Disease in Childhood and Journal of Inherited Metabolic Disease, and has written textbook chapters on genetic counselling, prenatal diagnosis, novel therapies for genetic disorders and inherited metabolic disorders. She has guided many postgraduate dissertations and has contributed to public awareness through television and newspaper features on rare genetic diseases.
Areas of Expertise :
- Inborn Errors of Metabolism
- Newborn Screening
- Prenatal Diagnosis
- Genetic Bone Disease
- Congenital Malformations and Chromosomal Anomalies
- Genetic Counselling
- Down Syndrome and Chromosomal Disorders
- Congenital Malformations
- Genetic Bone Disease (Skeletal Dysplasia)
- Lysosomal Storage Disorders
- Gaucher Disease
- Mucopolysaccharidosis
- Organic Acidemias
- Congenital Hypothyroidism
List of Treatments
- Inborn Errors of Metabolism
- Newborn Screening
- Prenatal Diagnosis
- Genetic Counselling
- Down Syndrome and Chromosomal Disorders
- Congenital Malformations
- Genetic Bone Disease (Skeletal Dysplasia)
- Lysosomal Storage Disorders
- Gaucher Disease
- Mucopolysaccharidosis
- Organic Acidemias
- Congenital Hypothyroidism
- Congenital Adrenal Hyperplasia
- Wilson Disease
Work Experience
Currently Working as Consultant - Clinical Genetics in the Clinical Genetics Department at P. D. Hinduja Hospital, Mahim, Mumbai, India.
Past Experience :
- Associate Professor of Paediatrics - Seth GS Medical College and KEM Hospital, Mumbai (10 years)
- Lecturer in Paediatrics - Seth GS Medical College and KEM Hospital, Mumbai (6 years)
- Research Scientist, Study of Malformations and Down Syndrome in India - Department of Atomic Energy, Bombay (1994-1995)
Education & Training
- MBBS - University of Bombay, 1989
- DCH - College of Physicians and Surgeons, 1993
- MD (Paediatrics) - University of Bombay, 1994
Awards & Recognition
- Principal Investigator - ICMR Task Force multicentric study on Newborn Screening for Congenital Hypothyroidism and Congenital Adrenal Hyperplasia
- Principal Investigator - Phase 3 multinational study in Gaucher Disease Type 1 (EDGE)
- Numerous publications in Indian Pediatrics, American Journal of Medical Genetics, Archives of Disease in Childhood and other journals
- Book chapters on genetic counselling, prenatal diagnosis and inherited metabolic disorders
Associated Hospitals
🏨 P. D. Hinduja Hospital, Mahim, Mumbai
Location
📌
P. D. Hinduja Hospital, Mahim, Mumbai, India
Frequently Asked Questions
Where does Dr. Mamta Muranjan practice?
Dr. Mamta Muranjan practises as Consultant - Clinical Genetics at P. D. Hinduja Hospital, Mahim, Mumbai.
What does Dr. Mamta Muranjan specialise in?
She specialises in inborn errors of metabolism, newborn screening, prenatal diagnosis, genetic bone disease and chromosomal anomalies.
How much experience does Dr. Mamta Muranjan have?
Dr. Mamta Muranjan has more than 30 years of experience in paediatrics, including 16 years in clinical genetics.
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