Department of Medical Genetics

Medical Genetics

The Department of Medical Genetics at Apollo Adlux Hospital is a specialised centre dedicated to the diagnosis, management, and counselling of individuals and families affected by genetic and inherited disorders. Combining cutting-edge molecular diagnostics with compassionate patient care, the department offers a comprehensive range of services spanning prenatal and postnatal genetic evaluation, dysmorphology assessment, cytogenetics, and advanced genomic interpretation.

Our team works at the intersection of clinical medicine and modern genomic science, providing accurate variant analysis and tailored management plans for conditions including inborn errors of metabolism, skeletal dysplasias, chromosomal abnormalities, and rare inherited syndromes. Through a multidisciplinary approach, we ensure that every patient — from newborns identified through neonatal screening to adults seeking answers for complex familial conditions — receives personalised, evidence-based care.

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Scope of Services

Scope of Services
  • Paediatric & Rare Diseases: Diagnosis of rare diseases, dysmorphology, inborn errors of metabolism (IEM), newborn screening, autism, developmental delay, intellectual disability, skeletal dysplasias, and growth disorders.
  • Fetal & Reproductive Genetics: Evaluation of fetal anomalies, prenatal and preconception counseling, recurrent pregnancy loss, infertility evaluation, guidance for NIPT & invasive testing (CVS/Amniocentesis).
  • Neurogenetics & Adult Care: Managing neurogenetic disorders: ataxias and muscle dystrophies.
  • Advanced Genomic Services: Expert interpretation of exome and genome sequencing.
  • Oncogenetics

Get to Know our Team of Experts

doctor

Dr. Sarath R S

Consultant

MBBS, DNB Paediatrics, MD Paediatrics, DM Medical Genetics

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