Dr. Moni T Bhatia
Noble Heart and Super Specialty Hospital
Personal Statement
I'm a caring, skilled professional, dedicated to simplifying what is often a very complicated and confusing area of health care...read more
Doctor Information
Speciality
- Geneticist
Other treatment areas
- Fetal Medicine
- Geneticist
Education
- MBBS , Lady Hardinge Medical College, New Delhi , 2004
- MD - Obstetrics & Gynaecology , Vardhman Mahavir Medical College & Safdarjung Hospital, Delhi , 2010
- DM Medical Genetics , Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow , 2014
Past Experience
- Junior resident at Safdarjung Hospital
- Senior resident at Sanjay Gandhi Postgraduate institute of medical sciences
- Assocaite consultant at Sir Gangaram hospital
- Senior geneticist and fetal medicine specialist at Noble heart and superspeciality hospital
Languages spoken
- English
- Hindi
Professional Memberships
- Indian Medical association life membership
- Haryana Obstetrics and Gynae society life membership
- Indian academy of medical genetics life membership
- Society of fetal medicine, life membership
- FOGSI Delhi branch life membership
Clinic Location
Plot Number-2, Raj Garden, Delhi Bye-Pass Chowk, Landmark: Near Apsara Cafe, Rohtak
Clinic of Dr. Moni T
| Clinic's Name | Fees |
|---|---|
| Noble Heart and Super Specialty Hospital | ₹ 1,200 |
Book Clinic Appointment with Dr. Moni T Bhatia
Noble Heart and Super Specialty Hospital
Question and Answers
Gunjan
female • 28 Year Old • Jan 24, 2020 • Chandigarh
Dual test in pregnancy result 1: 514 my doctor said it intermediate risk. What type of genetic disorder may be in child.
Moni Tuteja Bhatia
4 years ago
Hi lybrate-user. It is a risk for down syndrome. So there is 1 in 514 chance of down syndrome. 513 babies will be normal. It is a chromosomal disorder with mental retard ...read full answer
Amiya Jalvi
male • 22 Year Old • Aug 29, 2019 • Mumbai
I am having a b6pd deficiency. Can I take biotin 10,000 mcg caps? Will it cause any harm or its safe to consume.
Moni Tuteja Bhatia
4 years ago
Hello lybrate-user. Treatment can be given only after seeing the reports. Depends whether it is biotinidase deficiency or something else all the best.
Sidharth
male • 20 Year Old • Aug 14, 2019 • Bhubaneswar
I am 20 years old male. I recently noticed a brown ring around the iris of both my eyes. I was concerned if it was kf rings found in patients with wilson's disease. I ha ...read more
Poonam Singh Gambhir
4 years ago
First you consult an ophthalmologist and get eye examination done to confirm whether it is actually kf ring or something else. Then accordingly further consult a genetic ...read full answer
Aashish Mishra
male • 6 Year Old • Jul 02, 2019 • Raipur
Hi Sir, My 5 years child has a problem with his bone joints. All the joints have abnormal growth. Doctor said there is no solution of the same and this is the genetic pr ...read more
Moni Tuteja Bhatia
4 years ago
Hello lybrate-user. You need to consult a geneticist. Need to see all the x-rays and the child to consider further genetic testing. Thereafter only we will be able to ad ...read full answer
Swathi
female • 26 Year Old • Jan 06, 2018 • Hyderabad
I have down syndrome with trisomy 14/21, can tell me risk about these. One baby is died after 28 days she is positive in down syndrome. Again when I was conceived the ch ...read more
Poonam Singh Gambhir
6 years ago
I think you are balanced translocation carrier for chromosome 14/21. In this case in each pregnancy you need to go for amniocentesis at 16 weeks pregnancy to diagnose wh ...read full answer