Best Hospital Near me ChennaiImage
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.
- Genetic Counselling
- Chromosomal Microarray Analysis (CMA)
- Next-Generation Sequencing (NGS)
- Carrier Screening
Genetic Counselling
Comprehensive counselling helps patients and families understand genetic risks, inheritance patterns, implications of test results, and possible preventive strategies. Personalised plans empower patients to make informed choices about health and family planning.
Chromosomal Microarray Analysis (CMA)
Detects chromosomal abnormalities linked to developmental delay, intellectual disability, and congenital anomalies. Provides high-resolution detection of deletions, duplications, and aneuploidies.
Next-Generation Sequencing (NGS)
Enables deep analysis of multiple genes at once, allowing accurate identification of mutations responsible for inherited disorders. Ideal for diagnosing complex genetic syndromes.
Carrier Screening
Assesses couples for the risk of passing genetic conditions to their children, enabling informed reproductive decisions and early intervention planning.
- Congenital Disorders
- Hereditary Cancers
- Neurodevelopmental Disorders
- Metabolic Disorders
- Neuromuscular Disorders
- Ophthalmic and Auditory Genetic Disorders
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.
- Whole Exome Sequencing (WES)
- Targeted Gene Panels
- Carrier Screening Panels
- Non-Invasive Prenatal Testing (NIPT)
- Preimplantation Genetic Diagnosis (PGD)
- Karyotyping
- Metabolic Screening Panels
×
