I am a Consultant Geneticist and Consultant Paediatrician with extensive experience at the intersection of clinical genetics and pediatric medicine. Over the years, I have worked with a diverse patient population, with a strong focus on reproductive genetics, recurrent pregnancy loss, and infertility, where I integrate advanced diagnostic insights to guide precision care and improve outcomes for couples.
My pediatric practice is dedicated to the diagnosis and management of complex metabolic disorders, bringing together genetic knowledge and evidence-based pediatric care to optimize long-term health. I am deeply committed to advancing awareness and accessibility of genetic medicine, while fostering multidisciplinary collaboration to provide holistic, patient-centered solutions.
With a track record of blending clinical acumen, research insights, and compassionate care, I strive to empower families with clarity, actionable treatment pathways, and hope for the future.
Lead clinician in the Department of Medical Genetics with a sub-specialty in Inherited and Metabolic Disorders, responsible for diagnosing, interpreting, and managing genetic and metabolic conditions in neonatal, pediatric and prenatal settings.
Expert in genetic test planning—from chromosome-level assays to whole-genome sequencing—including post-test variant analysis and risk estimation for patients and families.
Provide genetic counselling across multiple specialties (Obstetrics & Gynaecology, Neonatology, Paediatrics, Dermatology, Ophthalmology, ENT, Oncology, Orthopaedics) supporting patients with inherited disorders and helping them understand recurrence risks, preventative options, and treatment pathways.
Manage inborn errors of metabolism: coordinate metabolic testing, interpret results, guide therapeutic/dietary interventions, and follow up longitudinally in paediatric populations.
Founder & Lead Clinician at The NxGen, Prabhadevi, Mumbai — a child‐health care centre dedicated to comprehensive paediatric and genetic services.
The clinic is committed to delivering a child‐friendly environment with a focus on patient and family-centred care, where both common paediatric concerns and complex genetic and metabolic disorders are managed under one roof.
Known for clear communication, detailed explanations, and a compassionate approach, The NxGen aims to build trust and empower parents/caregivers with knowledge throughout their child’s healthcare journey.
Serving as Consultant Clinical & Metabolic Geneticist with the Sujanan Program at Lilac Insights, Mumbai, where I lead metabolic genetics diagnostics, newborn screening and genetic counselling services.
Involved in the development and interpretation of advanced metabolic panels (including exome/NGS-based testing, lysosomal and peroxisomal disorders) to guide both acute and long-term management in inherited metabolic disorders.
Contribute to fetal autopsy services, helping clarify causes of fetal demise, recurrent anomalies or genetic/metabolic syndromes, with risk assessment and counseling for future pregnancies.
Collaborate in multidisciplinary teams (including metabolic dietitians, genetic counsellors) to ensure comprehensive patient-centred care—from diagnosis, through dietary and medical management, to family counselling.
HMX Genetics, Harvard University
HMX Genetics, Harvard University