Dr.Hemlata Wadhwani Bhatia

Dr.Hemlata Wadhwani Bhatia

Consultant
Speciality - Medical Genetics Clinic
Memberships:
  • Delhi Medical Council
  • Indian Academy of Paediatrics (A-0265)

PROFESSIONAL JOURNEY

Work Experience:
  • Dr.Hemlata Wadhwani Bhatia is a Consultant in Medical Genetics Clinic at Sri Balaji Action Medical Institute, Paschim Vihar, New Delhi and has 8 years of experience in this field.
  • She has expertise in Management of genetic disorders in children (single gene and chromosomal both) Intellectual disability / autism/ mental retardation, Dysmorphology and malformations, Metabolic disorders in children – work up and their treatment.
  • Management of pregnant ladies with positive biochemical screening (double marker, triple marker, and quadruple marker test) during pregnancy and ultrasound abnormalities in the fetus.
  • Recurrent abortions – workup and management
  • Prenatal diagnosis for various disorders including genetic, metabolic, fetal abnormalities, congenital infections, skeletal dysplasias, etc.
  • Workup, predictive testing and counseling of genetic disorders in adults like deafness, blindness, movement disorders, muscular dystrophies, skin diseases, Huntington’s disease, cancers, Charcot Marie Tooth disease, etc..
  • Max Super Speciality Hospital, Shalimar Bagh, New Delhi,
Education & Training:
  • M.B.B.S (MAMC), D.C.H. (SJH),
  • Fellowship in Medical Genetics (SGRH)
  • ICMR Certificate Course in Clinical Genetics (SGPGI, Lucknow)
  • Fellowship in Rare Disorders (Care for Rare Foundation, Germany)
Research & Publication:

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Speciality Interest:
  • Genetic disorders in Children like Thalassemia/ hemoglobinopathies
  • Muscular dystrophy
  • Mental Retardation
  • Seizures
  • Autism
  • Growth problems in children (genetic causes of failure to gain weight or short height or obesity)
  • Developmental delay
  • Speech delay
  • Metabolic disorders in children
  • Dysmorphism
  • In utero foetal anomalies like structural abnormalities in the foetus or Intrauterine growth restriction etc
  • High risk of Trisomy 21/13/18 in Double marker
  • Triple marker or Quadruple marker tests
  • Recurrent abortions
  • Adult onset genetic disorders like movement disorders
  • Myopathies
  • Cancer Genetics
Awards Information:
  • International Travel Merit Fellowship Award by Care for Rare Foundation, Europe for exceptional work in the field of Genetics (Awarded in Germany) in 2014

You Should Know About Sri Balaji Action Medical Institute :

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