Live Chat
Select Page
Yashoda Hospitals > Doctors > Pediatric Neurology > Dr Sarah Bailur
Dr Sarah Bailur

Dr Sarah Bailur

MBBS, DNB, FIGG, FSIAMG, MNT, FNM (Spain)

Department : Pediatric Neurology
Exp: 16 yrs
Designation: Consultant Medical Geneticist & Metabolic Specialist
Languages: English, Telugu, Hindi
Med Reg No: 66213

Day time OPD:
MON - SAT : 09:00 AM - 04:00 PM

Location: Hitec City
Book An Appointment Book Online Consultation
Download Profile

About the Doctor

Dr Sarah Bailur is a Consultant Medical Geneticist & Metabolic specialist working at Yashoda Hospitals, Hitec City.

Educational Qualifications

  • 2008 to 2012: M.B.B.S., Rajiv Gandhi University of Health Sciences.
  • 2010 to 2013: DNB, KIIMS, Hyderabad
  • 2014 to 2015: FICG, Indira Gandhi Institute of Child Health
  • 2015 to 2016: FSIAMG, NIIMS, Punjagutta
  • 2021: Metabolic Nutrition Traineeship, Emory University, USA.
  • FNM (Spain): St Joan de Déu Barcelona Hospital.

Experience

  • Dec 2021 – Feb 2026: Consultant Medical Geneticist & Metabolic Specialist, Faculty for Pediatric Postgraduate Training, Rainbow Children’s Hospital, Hyderabad
  • 2022 – 2024: Laboratory Molecular Geneticist, Unipath Diagnostics
  • Feb 2021 – Nov 2021: Consultant Medical Geneticist, AIG Hospitals
  • Visiting Consultant, Suraksha Children's Hospital; Visiting Consultant Ankura Hospital, Boduppal
  • Visiting consultant at UTAGE Neurology Centre
  • Paediatric Consultant at Paramitha Children Hospital
  • Consultant Paediatrician at Lakshmi Mukunda Hospital
  • March 2020 to Nov 2021 : Consultant Medical Geneticist Child and Genetic Private Clinic
  • Feb 2019 to Jan 2021: Consultant Medical and Metabolic Geneticist, Redcliffe Life Sciences
  • Nov 2017 to March 2020: Consultant Pediatrician & Medical Geneticist Kamineni Hospitals and Medical College
  • DNB Faculty at Kamineni Institute, Involved in training of Genetic counsellors and Pediatric postgraduate students
  • Consultant Medical Geneticist at Suraksha Children's Hospital and Utage Neurology Hospital, Hyderabad
  • July 2017 to Oct 2017: SIAMG Fellowship (Medical Genetics), Nizam’s Institute of Medical Sciences, Hyderabad, India
  • Aug 2016 to June 2017: Pediatrician and Clinical Geneticist, Disha Children’s Hospital, Hyderabad, India
  • July 2015 to July 2016: Worked as a senior registrar in the Department of Paediatrics.
  • July 2013 to July 2015: Paediatrician, Senior Registrar, Suraksha Children’s Hospital, Hyderabad, India.
  • March 2013 to May 2013: Worked as a senior registrar at Disha Children’s Hospital.
  • Jan 2010 to Jan 2013: DNB Training at Lotus Children’s Hospital & KIMS Hospital.
  • September 2009 to January 2010: Pediatric Registrar, Lotus Children’s Hospital, Hyderabad, India
  • March 2009 to September 2009: Duty Medical Officer – ICCU, Yashoda Hospital, Secunderabad, India
  • 2008: OPD assisting senior cardiologists, InnovaChildren's Heart Hospital, Hyderabad, India
  • June 2008 – July 2008: Observership in Psychiatry Department, Yenepoya medical college
  • March 2009 to September 2009: Duty Medical Officer – ICCU, Yashoda Hospital, Secunderabad, India.

Services offered

  • Pediatric Genetic Disorders/Syndromes
  • Inborn Errors of Metabolism
  • Storage Disorders
  • Antenatal Genetic Counselling
  • Periconception Genetic Counselling
  • Recurrent Pregnancy Loss
  • Infertility
  • Fetal Genetic Disorders
  • Consanguineous Couple Genetic Counselling
  • Preventive Genetics
  • Adult Genetics (stroke, neurodegenerative, polycystic kidney diseases)

Special Interest and Expertise

  • Short stature for Genetic Evaluation
  • Obesity for Genetic Evaluation
  • Cancer Genetics
  • Pretest Counselling
  • Post-test Counselling
  • Management of Genetic Disorders
  • Pre-implantation genetic testing
  • Counselling
Download Profile
  • Received grant for ISIEM Conference
  • Received a prize for a poster presentation at the CMC Vellore IAMG Conference.
  • Received prize for poster presentation at Jaipur for ISIEM Conference
  • National & International speaker – Invited for several conferences
  • Organized many conferences & workshops
  • Member of Indian Academy of Pediatrics , MEMBER OF INDIAN SOCIETY OF IEM
  • Gayathri I, Prashanth U, Sarah B, Annapurna S, Qurratulain H.Familial Acute Necrotising Encephalopathy: Evidence From Next-Generation Sequencing of Digenic Inheritance. Journal of Child Neurology. 2020:1-5 DOI:10.1177/0883073820902308
  • Sarah B, Ankita R, Gayathri I, Qurratulain H et al. Interaction of Multiple Gene Variants Might Be Associated with Autism Spectrum Disorders Unravelled by Next-Generation Sequencing Data. American Journal of Psychology and Behavioral Sciences 2019; 6(1): 1-7
    Interaction of Multiple Gene Variants Might Be Associated with Autism Spectrum Disorders Unraveled by Next-Generation Sequencing Data
  • Utility of next‑generation sequencing in genetic testing and counseling of disorders involving the musculoskeletal system—trends observed from a single genetic unit
    https://josronline.biomedcentral.com/articles/10.1186/s13018-022-02969-x
  • Manjushree Bhate, Merle Fernandes, Sirisha Senthil, Shruthi Bathula & Sarah Beilur (2022): Progeroid syndrome of De Barsy – a case report and review of ophthalmic literature, Ophthalmic Genetics
    doi: 10.1080/13816810.2022.2154810
  • Homocystinuria – MTHFR – case report Indian Journal of Pediatrics
  • Dave, M., Tayade, N., Lingappa, L. et al. Clinical, Biochemical and Molecular Findings of Two PMM2-CDG Cases from India. Ind J Clin Biochem (2025). https://doi.org/10.1007/s12291-025- 01298-0
  • Bhate M, Pochaboina V, Varma R, Bailur S, Levin AV, Martin F. Ophthalmic manifestations of Cousin syndrome. Journal of the American Association for Paediatric Ophthalmology and Strabismus. 2025 Sep 18:104641.

Posters/Papers/Oral Presentations

  • Poster Presentation:
  • Neurotransmitter disorders – case series Congenital disorders of glycosylation – clinical and molecular and management – NEUROLOGY CONFERENCE
  • Glutaric aciduria – long-term outcome in later diagnosis – SERN METABOLIC MEETING ANGELMAN SYNDROME CASE SERIES – NEUROPEDICON
  • December 2015 - Prader-Willi conference Australia: Prader-Willi syndrome, presenter – Gayathri: Beckwith-Wiedemann syndrome – an imprinting defect disorder
  • June 5, 2023 – Lysosomal storage society conference , Bangalore - Sarah Bailur - Lysosomal storage disorders - Mannosidosis and Fucosidosia
  • July 5, 2022 – BGCI conference, Hyderabad – SMN, the evading neuron - Sarah Bailur
  • Dec 5, 2022 – SIAMG national conference – Sarah Bailur, Pitt Hopkins syndrome, CMC vellore
  • Dec 5, 2023 - SIAMG National conference DEE25 case series
  • Dec 5, 2024 – Mitochondrial disease – different faces of NDUFS1, myself – Ahmedabad, Gujarat.
  • Feb 2022 - Neurotransmitter defects
  • Joubert syndrome case series, myself, Rare disease conference at Hyderabad University – Dr Reddy’s Lifesciences
  • Sep 20 2024 - Mednik syndrome case report, ISIEM conference, Jaipur
  • Double trouble – 2 metabolic disorders coexisting, myself, ISIEM conference 2024 Jaipur
  • Isovaleric acidemia-treatment outcome, myself, ISIEM conference Jaipur 2024
  • Glutaric aciduria – genetic profile, clinical and management – case series – SIAMG conference 2025

FAQ's

    Dr Sarah Bailur holds the following qualifications: MBBS, DNB, FIGG, FSIAMG, MNT, FNM (Spain)

    Dr Sarah Bailur is a Consultant Medical Geneticist & Metabolic Specialist who is a specialist with expertise in genetic evaluation for obesity and cancer genetics. And she carries special expertise in providing pre-test counselling, post-test counselling, and management of genetic disorders.

    Dr Sarah Bailur practises at Yashoda Hospitals, Hitec City.

    You can schedule an appointment with Dr Sarah Bailur for both an online video consultation and an OPD consultation by visiting her profile on Yashoda Hospitals.





      •

      Book an appointment
      in 2 minutes