Home Doctors Dr Surya Balakrishnan

    Dr Surya Balakrishnan

    Medical Genetics

    10+ Years Experience

    DNB Super specialty – Medical Genetics (NIMS, Hyderabad) DNB Internal Medicine (Apollo Main Hospitals, Chennai) MBBS – (Kempegowda Institute of Medical sciences, Bengaluru)

    Jubilee Hills, Hyderabad

    Telugu, English, Hindi, Tamil, Kannada, Malayalam

    MON-SAT

    Overview

    Dr. Surya Balakrishnan is a well-known Genetic Expert in Hyderabad, currently associated with Apollo Hospitals. She holds her DNB Super Specialty in Medical Genetics from NIMS, Hyderabad. She has been working in the field of Genetics for the last 10 years. She has been actively involved in the Diagnosis, Genetic Counseling and management of various genetic disorders. Her special area of interest is prenatal diagnosis of various genetic and non-genetic disorders of all streams of medicine i.e.; Neurology, Hematology, Cardiology, Gastroenterology and Pediatrics. 

    The doctor has actively engaged and gained lot of exposure by evaluating a variety of patients with all types of genetic disorders in the Outpatient for more than 10 years of developmental delay, intellectual disability, neurologic disorders, muscular dystrophy, myopathy, other neuromuscular disorders, short stature, skeletal dysplasias, congenital heart disease, cardiomyopathy, genetic disorders of skin, eye, deafness, immunodeficiency, genetic hemolytic anemias, bleeding disorders etc. 

    Registration No: 10954 

    Education

    Lifetime member at Society for Indian academy of Medical Genetics [SIAMG] – Membership ID – L/M-048 

    Experience
    • Senior Clinical Geneticist at Center for cellular & Molecular Biology [CCMB] – 3 Years
    • Managed Clinical Genetic outpatient center & Genetic diagnostic laboratory, Quality control & Training of dissertation students
    Special Interests

    Neurogenetics, Onco-genetics & Pediatric genetics 

    Research
    • Balakrishnan S, Aggarwal S, Muthulakshmi M, Meena AK, Borgohain R, Mridula KR, Yareeda S, Ranganath P, Dalal A. Clinical and Molecular Spectrum of Degenerative Cerebellar Ataxia: A Single Centre Study. Neurol India 2022; 70:934-42
    • Balakrishnan S, Ranganath P. Report of an unusual association of hydro syringomyelia with Gabriele-de Vries syndrome in an Asian-Indian patient. Clin Dysmorphol. 2021 Oct 1;30(4):204-206. doi: 10.1097/MCD.0000000000000385. PMID: 34456245.
    • Vineeth, V.S., Das Bhowmik, A., Balakrishnan, S. et al. Homozygous PCDH12 variants result in phenotype of cerebellar ataxia, dystonia, retinopathy, and dysmorphism. J Hum Genet 64, 183–189 (2019).
    • Narayanan DL, Ranganath P, Balakrishnan S, Dalal A. Mosaic paternal uniparental isodisomy of 15q11-q13 region causing Angelman phenotype. Clin Dysmorphol. 2019 Oct;28(4):202-204.
    • Babu J, Balakrishnan S. Muir–Torre syndrome – An Indian case report. Int J Mol Immune Oncol 2021;6(2):93-6
    Doctor Awards

    Certificate Of Achievement in Cancer Genomics and Precision Oncology (Harvard University, HMX Pro) 

    Dr Surya Balakrishnan

    Medical Genetics

    10+ Years Experience

    DNB Super specialty – Medical Genetics (NIMS, Hyderabad) DNB Internal Medicine (Apollo Main Hospitals, Chennai) MBBS – (Kempegowda Institute of Medical sciences, Bengaluru)

    Telugu, English, Hindi, Tamil, Kannada, Malayalam

    MON-SAT

    -

    Overview

    Dr. Surya Balakrishnan is a well-known Genetic Expert in Hyderabad, currently associated with Apollo Hospitals. She holds her DNB Super Specialty in Medical Genetics from NIMS, Hyderabad. She has been working in the field of Genetics for the last 10 years. She has been actively involved in the Diagnosis, Genetic Counseling and management of various genetic disorders. Her special area of interest is prenatal diagnosis of various genetic and non-genetic disorders of all streams of medicine i.e.; Neurology, Hematology, Cardiology, Gastroenterology and Pediatrics. 

    The doctor has actively engaged and gained lot of exposure by evaluating a variety of patients with all types of genetic disorders in the Outpatient for more than 10 years of developmental delay, intellectual disability, neurologic disorders, muscular dystrophy, myopathy, other neuromuscular disorders, short stature, skeletal dysplasias, congenital heart disease, cardiomyopathy, genetic disorders of skin, eye, deafness, immunodeficiency, genetic hemolytic anemias, bleeding disorders etc. 

    Registration No: 10954 

    Education

    Lifetime member at Society for Indian academy of Medical Genetics [SIAMG] – Membership ID – L/M-048 

    Experience
    • Senior Clinical Geneticist at Center for cellular & Molecular Biology [CCMB] – 3 Years
    • Managed Clinical Genetic outpatient center & Genetic diagnostic laboratory, Quality control & Training of dissertation students
    Special Interests

    Neurogenetics, Onco-genetics & Pediatric genetics 

    Doctor Awards
    Dr Surya Balakrishnan

    Certificate Of Achievement in Cancer Genomics and Precision Oncology (Harvard University, HMX Pro) 

    Research
    • Balakrishnan S, Aggarwal S, Muthulakshmi M, Meena AK, Borgohain R, Mridula KR, Yareeda S, Ranganath P, Dalal A. Clinical and Molecular Spectrum of Degenerative Cerebellar Ataxia: A Single Centre Study. Neurol India 2022; 70:934-42
    • Balakrishnan S, Ranganath P. Report of an unusual association of hydro syringomyelia with Gabriele-de Vries syndrome in an Asian-Indian patient. Clin Dysmorphol. 2021 Oct 1;30(4):204-206. doi: 10.1097/MCD.0000000000000385. PMID: 34456245.
    • Vineeth, V.S., Das Bhowmik, A., Balakrishnan, S. et al. Homozygous PCDH12 variants result in phenotype of cerebellar ataxia, dystonia, retinopathy, and dysmorphism. J Hum Genet 64, 183–189 (2019).
    • Narayanan DL, Ranganath P, Balakrishnan S, Dalal A. Mosaic paternal uniparental isodisomy of 15q11-q13 region causing Angelman phenotype. Clin Dysmorphol. 2019 Oct;28(4):202-204.
    • Babu J, Balakrishnan S. Muir–Torre syndrome – An Indian case report. Int J Mol Immune Oncol 2021;6(2):93-6
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