The Apollo Centre of Genomic Medicine, Mumbai is renowned for providing comprehensive genetic care, combining advanced diagnostics, personalised counseling, and cutting-edge treatments. We focus on helping patients understand, manage, and prevent genetic disorders with compassion, precision, and the latest technology.
Best Hospital for Medical Genetics in Mumbai - Apollo Hospitals
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Apollo Centre of Genomic Medicine – Advanced Genetic Care You Can Trust
The department of Genetic Medicine at Apollo Hospitals Mumbai stands as one of the best centres for genetic services in the region, offering world-class diagnostics, counseling, and management of inherited conditions. With decades of expertise, our centre specialises in advanced genetic testing technologies and clinical genetic counseling, enabling early diagnosis and personalised interventions.
Our modern infrastructure includes state-of-the-art Genetic Labs, Chromosomal Microarray platforms, and Next-Generation Sequencing (NGS) facilities. This ensures accurate diagnosis, rapid reporting, and holistic care from assessment to long-term management. Whether it is prenatal screening, cancer risk assessment, or management of rare genetic disorders, Apollo Centre of Genomic Medicine is your trusted partner in genetic health.
Choose Apollo Hospitals Mumbai – your premier destination for precision genetic care and superior health outcomes.
Expert Medical Genetics Team – Apollo Hospitals Mumbai
At Apollo Hospitals Mumbai, recognised as a top centre for genetic medicine, our expert team includes highly skilled and experienced geneticists, counselors, and laboratory scientists dedicated to advancing patient care. Key specialists include:
Our specialists provide personalised consultations, guiding patients and families through complex genetic health decisions, preventive strategies, and management plans. We are committed to delivering compassionate, evidence-based, and precise care.
Top Procedures and Services
Types of Genetic Disorders Treated
Congenital Disorders
Structural or functional abnormalities present from birth, managed with precise diagnosis and multidisciplinary care.
Hereditary Cancers
Risk evaluation for familial cancers (breast, ovarian, colorectal) allowing early detection and preventive strategies.
Neurodevelopmental Disorders
Conditions like autism spectrum disorders, intellectual disabilities, and epilepsy assessed for genetic causes.
Metabolic Disorders
Inherited metabolic conditions such as phenylketonuria, managed through newborn screening and early intervention.
Neuromuscular Disorders
Inherited disorders like muscular dystrophies, evaluated through comprehensive genetic testing and counseling.
Ophthalmic and Auditory Genetic Disorders
Early diagnosis and management of inherited blindness and deafness improving patient outcomes.
Sub-Specialities in Medical Genetics
Prenatal Genetic Testing
Non-invasive and invasive tests performed to detect genetic abnormalities in the foetus early in pregnancy. These tests help in early detection of chromosomal disorders, enabling better management decisions.
Cancer Genetics
Personalised risk assessment and genetic testing for hereditary cancer syndromes help in early detection and preventive interventions.
Newborn Screening
A critical service to detect genetic and metabolic disorders at birth, allowing immediate management to prevent serious complications.
Neurogenetics
Evaluation of inherited neurological conditions such as epilepsy, neuromuscular disorders, and neurodevelopmental delay using advanced genetic diagnostics.
Cutting-Edge Technology and Advantages
Next-Generation Sequencing (NGS)
NGS allows simultaneous sequencing of thousands of genes, providing comprehensive genetic profiles with high accuracy and fast turnaround times.
Chromosomal Microarray Analysis (CMA)
Provides detailed assessment of chromosomal variations, detecting microdeletions and duplications undetectable by traditional karyotyping.
Fluorescence In Situ Hybridization (FISH)
Visualises specific DNA sequences on chromosomes, helping detect structural anomalies in critical regions linked to genetic disorders.
