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Dr. Ashutosh Gupta

Dr. Ashutosh Gupta -  Fetal Medicine, Genetics Doctor in Gurgaon, India
Designation: Head – Fetal Medicine
Specialty :
Fetal Medicine, Genetics
Location :
Gurugram
Nationality :
Indian
Languages Spoken :
English, Hindi
Gender :
Male
Artemis Hospitals
Profile:

Qualifications:

MBBS, MS (OBGYN), DM (Medical Genetics)
Medical School: MBBS - SNMC Jodhpur, Rajasthan
Post Graduate Programs: MS - Obstetrics & Gynecology; NCSB Medical College; Jabalpur, MP
Graduate Programs: DM (Medical Genetics) SGPGIMS, Lucknow
M.B.B.S. – Dr S.N. Medical College, Jodhpur, 2000 
Post Graduation – M.S. (Obstetrics & Gynecology), NSCB Medical College, 2005 
Super Specialization – D.M. (Medical Genetics), SGPGIMS, Lucknow, 2009 Fetal Medicine Fellowship – Programme 

Specializations:

Fetal Medicine & Clinical Geneticist  
Prenatal invasive testing of the fetus (Amniocentesis, CVS, Intrauterine transfusions, Multifetal pregnancy reductions, Shunt procedures – Vesicoamniotic shunting); experience of more than 2000 procedures Antenatal Obstetric ultrasounds (Nuchal, Anomaly, Color doppler, Biophysical profile, Fetal Echocardiography) Genetic counselling Clinical Geneticist – Dysmorphology, Prenatal diagnosis for both chromosomal and non-chromosomal syndromes, Molecular tests and prenatal diagnosis for genetic diseases.

Memberships: 

FOGSI
AOGD

Honors & Awards:

Ex Member – State Advisory Board under Pre-Conception & PNDT, Directorate of Family Welfare, Government of Delhi 
Ex Co Chairperson for AOGD subcommittee on Fetal medicine & Genetic committee; New Delhi

Clinical Focus:

Fetal Medicine & Clinical Geneticist  

Procedures:

Prenatal invasive testing of the fetus (Amniocentesis, CVS, Intrauterine transfusions, Multifetal pregnancy reductions, Shunt procedures – Vesicoamniotic shunting); experience of more than 2000 procedures Antenatal Obstetric ultrasounds (Nuchal, Anomaly, Color doppler, Biophysical profile, Fetal Echocardiography) Genetic counselling Clinical Geneticist – Dysmorphology, Prenatal diagnosis for both chromosomal and non-chromosomal syndromes, Molecular tests and prenatal diagnosis for genetic diseases. 

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