Dr. Sangeeta

Dr. Sangeeta

MBBS, DNB OBS &GYNAE, DGO, DNB Medical Genetics

Dr. Sangeeta a postgraduate from Maharaja Agrasen Hospital, Punjabi Bagh, New Delhi. She has worked at Max Hospital , Saket. She did her three years super specialisation training in Medical Genetics from Sir Ganga Ram Hospital, New Delhi under Dr. I.C. Verma and Dr. Ratna Dua Puri.

During her training, she has dealt with a broad spectrum of patients with various Genetic concerns like high risk biochemical screen in pregnancy, congenital malformations on ultrasounds, recurrent pregnancy losses, children and adults with chromosomal, syndromic , single gene disorders and various inborn errors of metabolism. She did her Thesis work on Outcome of pregnancies with increased nuchal translucency in first trimester. She has publications in International and National Journals of Medical Genetics and Fetal Medicine. She has done National courses in Biochemical Genetics and Molecular Genetics at CDFD, Hyderabad, Population Genetics at NIBMG, Kolkata.

Research articles/Papers published in  journals:

Sr.No. Title of research article Name of Journal Whether author/co author Month and year of publication
1. Genetic disorders in children with hepatosplenomegaly Medic Mentor Author Vol.1,no.6,Dec-Jan.2016
2. Sengers syndrome in Asian Indians-two novel mutations and variant phenotype Tranlational Science of Rare Diseases Author Vol.2,no.3-4,pp.157-164,2017
3. LG9 Associated Gillessen-Kaesbach–Nishimura Syndrome (GIKANIS): An Uncommon Aetiology of Enlarged Foetal Kidneys

 

Journal of Fetal Medicine Co author 10.1007/s40556-018-0183-1.2018
4. Mutation- proved Clouston syndrome in a large Indian family with Variant phenotype Indian Journal of Dermatology Author Accepted for Publication-Manuscript no.IJD_510_17

Papers/Posters  published/presented in  National or International conferences:

Sr.No. Title of Paper Name of conference City Date/Year
1. To study the outcome of foetuses with increased nuchal translucency in first trimester Annual congress of Society of Fetal Medicine Kolkata 9th-11th Sept.2016
2. Clinical profile of patients with 22q deletion syndrome 3rd International Conference on birth defects New Delhi 7th-10th Dec.2016
3. The emergence of nuclear genes  encoded mitochondrial  disorders in era of next generation sequencing 4th Conference ISIEM Chennai 10th-12th Feb.2017
4. To study the outcome of foetuses with increased nuchal translucency in first trimester-Extended study International Congress of Society of fetal Medicine Gurugram 1st-3rd Sept.2017

Lifetime Membership of societies:

• Indian Fertility society(IFS)
• Federation of Obstetric and Gynecological Societies of India (FOGSI)
• Society of Fetal Medicine (SFM)
• Society of Indian Journal of Medical Genetics (SIAMG)
• Indian Society of Inborn errors of Metabolism (ISIEM)