MBBS, DNB (Paediatrics), Fellowship in Paediatric Genetics

OPD Timings:

Tuesday, Thursday and Saturday: 03:00 pm to 05:00 pm

    Qualifications & Education:

    • Fellowship in Paediatric Genetics – Indira Gandhi Institute of Child Health, Bengaluru (2023–2024)
    • DNB (Paediatrics) – Rainbow Children's Hospital, Banjara Hills, Hyderabad (2020–2023)
    • MBBS – Gandhi Medical College, Secunderabad (2013–2018)

    Areas of Expertise:

    • Clinical Genetics
    • Paediatric Genetic Disorders
    • Dysmorphology Evaluation
    • Prenatal & Postnatal Genetic Diagnosis
    • Genetic Counselling
    • Congenital Anomalies Evaluation
    • Rare Metabolic Disorders
    • Genomic Sequencing & Variant Interpretation

    Clinical Expertise:

    • Evaluation and management of common and rare genetic disorders
    • Genetic counselling for affected children and families
    • Prenatal counselling for abnormal antenatal scans
    • Interpretation of genomic sequencing and genetic variants
    • Diagnosis and management of inherited metabolic disorders
    • Enzyme replacement therapy for Gaucher disease, Pompe disease, Niemann-Pick disease, and Mucopolysaccharidosis
    • Multidisciplinary management of children with genetic disorders
    • Interpretation of Variants of Uncertain Significance (VUS)

    Professional Experience:

    • Consultant – Clinical Geneticist, KIMS Hospitals, Mahadevapura, Bengaluru (2026–Present)
    • Consultant – Clinical Geneticist, MedGenome Labs, Bengaluru (2025–Present)
    • Specialist – Paediatrics & Clinical Genetics, BabyMD Clinic, Bengaluru
    • Specialist – Paediatrics & Clinical Genetics, Healthland Clinic, Bengaluru
    • Paediatrician & Clinical Geneticist, Aster Hospital, Whitefield, Bengaluru
    • DNB Resident – Paediatrics, Rainbow Children's Hospital, Hyderabad

    Research & Publications:

    • Poster Presentation – Asian Congress of Pediatric Nephrology (2023)
      • Unveiling Schimke Immuno-Osseous Dysplasia: A Case Report of Disproportionate Short Stature with Renal Dysfunction
    • Paper Presentation – Pediatric Ophthalmology and Strabismology Network (2024)
      • Ophthalmological Findings in 71 Molecularly Confirmed Individuals with Gaucher Disease from a Tertiary Genetic Center
    • Poster Presentation – 23rd National Conference of Pediatric Rheumatology (2025)
      • Clinical Insights into Childhood A20 Haploinsufficiency
    • Poster Presentation – 23rd National Conference of Pediatric Rheumatology (2025)
      • Unmasking NOMID in an Infant with Developmental Delay

    Certifications:

    • Postgraduate Program in Pediatric Nutrition – Boston, USA (2021)
    • Clinical Interpretation of Whole Genome Sequences – Karkinos (2025)
    • Pediatric Advanced Life Support (PALS)
    • Basic Life Support (BLS)
    • Advanced Cardiovascular Life Support (ACLS)

    Academic Contributions:

    • Active faculty for teaching sessions on genetic diagnosis and interpretation of genetic reports
    • Regular participant in academic presentations, workshops, and conferences in Clinical Genetics
    • Active participant in quizzes related to Paediatrics, Neonatology, Nephrology, Nutrition, and Metabolic Disorders

    Professional Interests:

    • Dysmorphology
    • Prenatal Genetics
    • Rare Genetic Disorders
    • Inherited Metabolic Diseases
    • Clinical Genomics

    Languages Known:

    English, Telugu, Kannada, and Hindi

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