Dr. Mamta Muranjan

Dr Mamta Muranjan is an exceptionally distinguished and authoritative Senior Consultant Clinical Geneticist and Paediatrician in Mumbai, bringing an incredible 37 years of clinical experience to the highly specialised field of rare childhood diseases.

She currently consults at premier institutions including SRCC Children Hospital and P D Hinduja Hospital. Possessing a formidable academic foundation, she holds an MD in Paediatrics and a DCH.

She is universally recognised as one of India's foremost authorities on clinical genetics, with profound expertise in managing rare inborn errors of metabolism (including enzyme replacement therapies), skeletal dysplasias, and complex chromosomal anomalies.

Deeply committed to pioneering genetic research and delivering highly empathetic patient care, she consults fluently in English and Hindi.

Specialty Areas, Conditions, and Treatments

Dr Mamta Muranjan provides highly precise, life-sustaining medical interventions and comprehensive genetic care for infants and children battling severe metabolic disorders, congenital anomalies, and rare genetic diseases across Mumbai.

Inborn Errors of Metabolism and Rare Diseases

Children diagnosed with rare, life-threatening inborn errors of metabolism (such as Gaucher disease, Pompe disease, or severe lysosomal storage disorders) demand elite, highly targeted systemic oversight. Dr Mamta provides authoritative metabolic care:

• Precision Enzyme Replacement Therapy (ERT) for Lysosomal Storage Disorders
• Advanced Metabolic Screening and Genotype-Phenotype Correlation
• Customised Medical Nutritional Therapy for Organic Acidemias

Prenatal Diagnosis and Congenital Malformations

Expecting parents with a strong family history of severe genetic disorders requiring urgent prenatal diagnosis, or infants born with complex, unexplained congenital malformations require highly empathetic and scientifically rigorous evaluation. Dr Mamta offers expert genetic management:

• Advanced Prenatal Genetic Screening and Risk Assessment
• Complex Dysmorphology and Teratology Assessment
• High-Risk Genetic Counselling for Families

Chromosomal Anomalies and Skeletal Dysplasia

Children suffering from severe, unexplained developmental delays, abnormal bone growth (such as skeletal dysplasia), or multisystemic conditions linked to chromosomal anomalies (like Down Syndrome) require precise, long-term developmental tracking. Dr Mamta provides elite genetic intervention:

• Complex Chromosomal Karyotyping and Microarray Analysis
• Genetic Bone Disease Diagnostics and Management
• Long-term Neurodevelopmental and Syndromic Tracking

Credentials and Trust Signals

Dr Mamta Muranjan possesses an incredibly robust and highly specialised academic foundation, representing the absolute highest echelons of paediatric and genetic training in India:

• MBBS from Seth GS Medical College and KEM Hospital, University of Bombay (1989)
• Diploma In Child Health (DCH) from the College of Physicians and Surgeons, Mumbai (1993)
• MD in Paediatrics from Seth GS Medical College and KEM Hospital, University of Bombay (1994)

Extensive Research, Academic Leadership, and Selected Publications

Demonstrating a massive clinical legacy spanning nearly four decades, Dr Mamta is a true pioneer in the field of Indian Clinical Genetics:

• Academic Authority: Serves as a Professor (Additional) of Paediatrics and the In-charge of the Genetic Clinic at the prestigious Seth GS Medical College & KEM Hospital, Mumbai, carrying over 25 years of postgraduate teaching experience.
• National Research Leadership: Served as the Principal Investigator for the Indian Council of Medical Research (ICMR) Task Force on Inborn Metabolic Diseases.
• Selected Landmark Publications: Dr Mamta has authored over 147 research papers in international journals. Some of her highly cited publications include:
  • "Impact of Enzyme Replacement Therapy on Patients with Late Onset Pompe Disease" (The Indian Journal of Pediatrics).
  • "Clinical, biochemical and molecular spectrum of acute neuronopathic type 2 Gaucher disease from India" (BMC Pediatrics).
  • "Development of national biobank for lysosomal storage disorders in India" (Orphanet Journal of Rare Diseases).

Professional Memberships

Dr Mamta holds esteemed leadership positions and memberships in elite national genetic and paediatric associations, reflecting her deep commitment to advancing rare disease management:

• Indian Society For Inborn Errors of Metabolism (ISIEM)
• Indian Academy of Paediatrics (IAP)
• Family Planning Association of India (FPAI)

Current Hospital Affiliations in Mumbai

Dr Mamta Muranjan currently consults as a leading Senior Consultant Clinical Geneticist at the following premier healthcare facilities:

• SRCC Children Hospital (Narayana Health), Mahalakshmi, Mumbai. (Consultation Fee: ₹3000)
• P. D Hinduja National Hospital And Medical Research Centre, Mahim West, Mumbai.

Book an Appointment with Dr Mamta Muranjan, Clinical Geneticist

For highly specialised enzyme replacement therapies, expert management of inborn errors of metabolism, and advanced prenatal genetic diagnosis, connect with the medical experts at HexaHealth to check availability and secure your priority appointment with Dr Mamta Muranjan.