Welcome to Prime Centre of Genetics & Fetal medicine

This is one of its kind centres in Haryana to provide Genetic counselling and Prenatal Diagnosis.

Monday - Friday
9:00 AM- 2:00 PM
Saturday
9:00 AM- 2:00 PM
Sunday
Closed
Emergency number
+91 8222 044 022
E-mail Address
info@primegenetics.in

Why choose us?

Our aim is not only to provide cure but also to counsel you for your current and future pregnancy and to guide you regarding other common genetic disorders. We strive to help you achieve your wellness goals for your baby and have a safe pregnancy.We offer an approach to manage pregnancies with fetal abnormalities and work in collaboration with your obstetrician.

Experience and Professionalism

We have a well trained geneticist and a fetal Medicine expert who has worked Prior with hospital Sir Ganga Ram Hospital, New Delhi. Our medical team has been managing patients with different genetic disorders.

Our Services

About Us

Our centre is one of its kind in Haryana and Punjab to deal with and treat genetic disorders and disorders of the fetus. It is established since January 2017. We have a doctor with high qualification and experience in the field of genetics and fetal medicine. At this centre you will be greeted by our trained staff and each and every patient is given personal attention with treatment and investigations ordered in accordance with the newest technology.

Frequently Asked Questions

Genetics is the study of genes and genetic variation.It is to understand the what causes the disease in the family.
All of us know that our body is made up of cells. Each cell contains a nucleus. Nucleus has the genetic make up of the individual in the form of chromosomes. All of us have 23 pairs of chromosomes. These chromosomes have tightly coiled DNA and on this DNA a number of genes reside. If nucleus is a book, then chromosome is a chapter in the book and gene is a particular line in that chapter.
It is important to understand the genetic problem in the family because it has multiple health implications for your family as a whole. When multiple family members have similar problem then genetic disease is suspected. Moreover when there are early deaths in childhood or in adulthood without any known cause suspect genetic disease. Developmental delay, autism, congenital heart disease, multiple miscarraige and pregnancy ultrasound showing any abnormality may also suggest some genetic cause.
Genetic test is a broad term. It encompasses broad range of testing to identify a disorder ranging from Sanger sequencing, next generation sequencing, multiplex ligation probe amplification, karyotype to microarray and so on. There is no such broad test. The type of test will depend on what disorder is suspected in you or your family member.
Prenatal screening is the investigation which is conducted in the pregnant women to determine the chance of baby having a specific chromosomal disorder. It is a screening test which means that it just tells you that you are at increased risk and warrants further testing. They are usually carried out in the first trimester or second trimester.
It is a type of non invasive screening test to detect Down syndrome babies. In this a simple blood sample is taken to determine the risk. It is a high efficiency screening test and is not a diagnostic test.There are various methods available for testing and needs to be determined by taking a proper history and examining all the documents of pregnancy.

Prime centre of genetics and fetal medicine

A one stop solution for all genetic disorders

Contact Us

Latest News

Testimonials

“It is one of the best superspeciality hospital with all the departments under one roof. Doctors here are very efficient and dedicated”
Mrs Komal
“Dr Moni Bhatia is well trained and an expert in her field. I found the answer to all my queries “
Mr Ashutosh
“Prime centre is a centre with the best quality care. I would highly recommend it”
Mr Jitender
“Treatment here is excellent and the staff and the doctors are very supportive here”
Mrs Priyanka
“Doctors and staff us very helpful and caring. I would highly recommend it to all”
Mrs Shashi

Our Mission

India is the country where the prevalence of communicable diseases is decreasing, so the focus is shifting to genetic disorders and congenital malformations. They are the important cause of morbidity and mortality in these individuals. So our aim is to detect these disorders early and allow early treatment of these disorders and to provide the prenatal diagnosis for the disorders for which the treatment is not available.

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