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Dr. Devi Saranya S

Dr. Devi Saranya S

Consultant – Medical Genetics

MBBS, MD ( Pediatrics), DM (Medical Genetics), MRCPCH
Speciality
Paediatrics
Languages
English, Malayalam, Hindi
Overview

Dr. Devi Saranya S is a Consultant Clinical Geneticist and Metabolic Physician with expertise in the diagnosis, management, genetic counselling and treatment of inherited disorders across all age groups. She completed her MD Pediatrics and DM in Medical Genetics from the All India Institute of Medical Sciences (AIIMS), New Delhi, one of India's premier institutes, and is also holds MRCPCH (UK) degree. Her clinical interests include rare genetic disorders, inborn errors of metabolism, neurogenetic disorders, dysmorphology, prenatal genetics, hereditary cancer syndromes, and genomic diagnostics. She has extensive experience in interpreting advanced genetic investigations, including exome sequencing, genome sequencing, chromosomal microarray, and prenatal genetic testing. Dr. Devi has authored multiple peer-reviewed publications in reputed international journals and has presented award-winning research at national conferences. She has been actively involved in multicentric clinical research and clinical trials in lysosomal storage disorders and other rare diseases. She believes in combining precision medicine with compassionate genetic counseling to help patients and families make informed healthcare decisions. Her practice focuses on delivering comprehensive genetic care from diagnosis to long-term management and family screening.

 

 

Area of expertise

• Clinical Genetics across pediatric and adult age groups
•  Rare genetic disorders
•  Inborn Errors of Metabolism (IEM)
•  Prenatal genetics and fetal anomaly evaluation
•  Genetic counseling and reproductive counseling
•  Dysmorphology evaluation
•  Neurogenetic disorders
•  Developmental delay, autism spectrum disorders, and intellectual disability genetics
•  Chromosomal disorders
•  Whole Exome Sequencing (WES), Whole Genome Sequencing (WGS), and genomic data interpretation
•  Hereditary cancer genetics
•  Lysosomal storage disorders
•  Skeletal dysplasias
•  Neuromuscular genetic disorders
•  Pharmacogenomics
•  Cascade family screening and preventive genomics
 

Awards and recognitions

•  First Prize – ISIEM Foundation Course on Inborn Errors of Metabolism (2025)
•  Second Prize – Oral Presentation, AIIMS Research Day (2025)
•  Second Prize – Poster Presentation, ISIEM Conference (2024)
•  Second Prize – NARCHI National Quiz (2024)
•  Harvard Medical School HMX Certification in Cancer Genomics and Precision Oncology (2024)
 

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