Fortis Hospital, Gurugram: Your Partner in Genetic Health

At Fortis Hospital, Gurugram, our Medical Genetics Department is dedicated to providing cutting-edge genetic services and personalized care. Our team of highly skilled geneticists, counselors, and healthcare professionals work collaboratively to offer comprehensive genetic evaluations, diagnostics, and treatments for a wide range of genetic conditions.

Led by Dr. Richa Soni, a renowned medical geneticist with expertise from AIIMS Delhi, our dedicated team at Fortis Hospital, Gurugram, provides comprehensive genetic services tailored to your unique needs. We offer advanced genetic evaluations, precise diagnostic testing, and personalized treatment plans for a wide range of hereditary conditions.

Our collaborative approach involves specialists from various fields to ensure comprehensive care. By harnessing cutting-edge technology and prioritizing patient-centric care, we empower individuals with genetic insights, enabling them to make informed decisions and manage their genetic health effectively.

 

Our Services
Prenatal and Preconception Genetics: We offer comprehensive counseling and testing for expectant parents and those planning to conceive, helping them understand the risks and options related to genetic conditions.

Pediatric Genetics: Our pediatric geneticists specialize in diagnosing and managing genetic disorders in children, providing early intervention and tailored treatment plans.

Adult Genetics: We provide genetic evaluations and counseling for adults, addressing concerns such as inherited diseases, familial cancer syndromes, and more.

Cancer Genetics: Our cancer genetics program offers risk assessment, genetic testing, and counseling for individuals with a family history of cancer, helping them make informed decisions about their health.

Pharmacogenomics: We utilize genetic information to guide personalized medication management, ensuring that patients receive the most effective and safe treatments based on their genetic makeup.

Our Team of Experts

FAQs

  • What is Medical Genetics?
    Medical genetics is the study of how genes influence our health and disease. It helps us understand why some people are more susceptible to certain illnesses while others are not. By examining our DNA, scientists can identify genetic variations that contribute to various health conditions. This knowledge can lead to earlier diagnosis, more effective treatments, and even preventive measures.
  • Common genetic disorders and their symptoms
    In India, a variety of genetic disorders affect people of all ages. Common conditions include sickle cell anemia, thalassemia, cystic fibrosis, beta thalassemia, phenylketonuria, muscular dystrophy, hemophilia, albinism, cleft lip and palate, and thalassaemia. These disorders can cause a range of symptoms, from mild to severe, and may require lifelong management
  • Genetic testing: What to expect
    Genetic testing is a process that examines your DNA to identify genetic variations that may be linked to certain health conditions. In India, genetic testing is becoming increasingly accessible and can provide valuable information about your risk for various diseases. The process typically involves a simple blood or saliva sample, followed by laboratory analysis. The results can help you make informed decisions about your health and well-being, such as lifestyle changes, preventive screenings, or treatment options.
  • Genetic counseling: What is it and when is it recommended?
    Genetic counseling is a process that provides information and support to individuals and families who are considering or have undergone genetic testing. Medical geneticists, play a crucial role in explaining the results of genetic tests, discussing the implications for health and family planning, and offering guidance on coping with genetic information. Genetic counseling is recommended for individuals with a family history of genetic disorders, those who are considering genetic testing, or those who have received a genetic diagnosis.
  • The role of genetics in personalized medicine
    Genetics plays a pivotal role in personalized medicine. By analyzing an individual's genetic makeup, healthcare providers can tailor treatments and preventive measures to their specific needs. This approach can lead to more effective outcomes, reduced side effects, and improved overall health. Genetic information can help identify individuals at risk for certain diseases, allowing for early intervention and targeted prevention strategies.
  • The future of medical genetics
    The future of medical genetics is promising and exciting. As technology continues to advance, genetic testing is becoming more accessible and affordable. This means that more people will have the opportunity to learn about their genetic predispositions and take proactive steps to improve their health. Additionally, researchers are making significant progress in understanding the complex interplay between genes and the environment, which will lead to more targeted and effective treatments for a wide range of diseases.
  • Cystic fibrosis: Causes, symptoms, and treatment options
    Cystic fibrosis (CF) is a genetic disorder that affects the lungs, pancreas, and other organs. It is caused by a mutation in the CFTR gene, which regulates the movement of salt and water in and out of cells. Symptoms of CF include persistent cough, frequent respiratory infections, thick mucus, difficulty breathing, salty-tasting sweat, and pancreatic insufficiency. While there is no cure for CF, treatments like mucus thinners, bronchodilators, antibiotics, and pancreatic enzymes can help manage symptoms and improve quality of life.
  • Sickle cell anemia: What you need to know
    Sickle cell anemia (SCA) is a genetic disorder that affects the red blood cells. It is caused by a mutation in the hemoglobin gene, which produces a protein that carries oxygen in the blood. In SCA, the mutation causes the red blood cells to become sickle-shaped, which can lead to a variety of health problems, including anemia, pain crises, and organ damage. If you or your family have a history of SCA, it's important to understand the genetics behind this condition and the available treatment options.
  • Huntington's disease: Diagnosis, management, and genetic counseling
    Huntington's disease (HD) is a genetic disorder that causes progressive nerve damage. It is caused by a mutation in the huntingtin gene, which is located on chromosome 4. Symptoms of HD typically begin in mid-life and include involuntary movements, cognitive decline, and emotional changes. If you have a family history of HD, genetic testing can help determine your risk of developing the condition. Early diagnosis and management can help improve quality of life for individuals with HD. Genetic counseling can also provide support and guidance to individuals and families affected by this disorder.
  • Autism spectrum disorder: Genetic factors and early intervention
    Autism spectrum disorder (ASD) is a complex neurodevelopmental condition that affects communication, behavior, and social interaction. While the exact causes of ASD are not fully understood, genetic factors play a significant role. Research suggests that multiple genes may contribute to the development of ASD. Early intervention is crucial for individuals with ASD as it can help improve communication, social skills, and behavior.
18th Annual Conference of AMPI( Northern Chapter)

We are glad to inform you that the Fortis Memorial Research Institute (FMRI), Gurugram will be hosting the 18th Annual Conference of AMPI-NC (AMPINC-CON2025) during 26th and 27th of April 2025. 

 

The Association of Medical Physicists of India (AMPI) was founded in 1976 and it has seven regional chapters including Northern Chapter. Objective of this association is to encourage the application of physics in medicine and providing a forum for medical physicists to exchange their ideas and dissemination of new knowledge in the form of annual conferences.

 

Established in 2013, Fortis Memorial Research Institute (FMRI), is located in the heart of Gurgaon.  Spanning an impressive 11-acre campus, FMRI is a premier multi-super-specialty quaternary care hospital having a total of 330 operating beds and completely equipped with cutting-edge technology to provide comprehensive care across a wide range of medical specialties.  It is a JCI and NABH accredited institution with NABL accredited laboratory services.

 

The Department of Radiation Oncology of FMRI has the privilege of commissioning the First MR Linac equipment in Northern India which is the latest high-end technology in radiation therapy.  Additionally, the department is equipped with state of art technologies with two linear accelerators (Elekta) and one brachytherapy equipment (Elekta/Microselectron V3).  Surface Guided Radiotherapy (SGRT/C-Rad)) has also been commissioned in the department recently.

 

The latest version of Gamma Knife (Elekta/Esprit) was commissioned under Neuro surgery department this year.  More than 100 patients have already been treated using this equipment.

 

FMRI is always on the front foot for promoting continuous medical education and academic activities. AMPINC-CON2025, the forthcoming conference of AMPI (Northern Chapter) will be one such event for sharing medical physics knowledge and radiotherapy practices from distinguished faculties and practising Medical Physicists across the country. 

 

Theme:  Adaptive Radiotherapy – Present and Future

Key topics covered:

-External Beam Radiotherapy

-Brachytherapy

-Medical Physics academic and research activities

-Application of Medical Physics in Imaging

-Application of Artificial Intelligence in Medical Physics

-Online and offline adaptive radiotherapy

-Radiation safety

 

Event Date:  26-04-2025 and 27-04-2025

Contact: +91-124-4962200 Ext 5155: Mobile No: +91-9971984695 & +91-9941634329

Organising Chairperson              

 Dr. Anil Kumar Anand, Senior Director & HOD, (Dept of Radiation Oncology)

 

Organising Secretary                    

Dr. Radhakrishnan B Nair, Chief Medical Physicist & RSO

 

FOR REGISTRATION PLEASE CLICK THE LINK BELOW 

Register now 

 

Abstract Guidelines

  • Registration is pre-requisite before submitting the abstract
  • Abstract should be typed in word doc format (Times New Roman font, size 12) not exceeding 500 words
  • Abstract should not have been submitted / presented / intended for presentation elsewhere before NCAMPIN-CON 2025.
  • The name of the presenting author should be mentioned first, followed by the names of other authors. The affiliations of all authors must be stated.
  • All abstracts will be reviewed by Scientific Committee and the presenting authors will be notified via email regarding acceptance.

 

Structure of the Abstract

  • Title
  • Objectives
  • Material and Methods
  • Results & Discussion
  • Conclusion
  • References
  • The last date for submission is 28th February 2025.
  • All abstracts must to be submitted by email to [email protected]

 

Payment Details

 Hospital Name  : Fortis Hospitals Limited 

Address  : Sector-44, Opp Huda City Centre Metro Station, Gurgaon-122002

Bank Name : The Hongkong and Shanghai Banking Corporation Ltd

Bank Address  : JMD Regent Square, Gurgaon –Mehrauli Road, DLF Phase II, Gurgaon-122001

A/C Holders Name (Name as per chq copy) :Fortis Hospitals Limited 

Account Number  : 054-031356-911

SWIFT CODE :HSBCINBB

IFSC Code :HSBC0110005

MICR Code :110039005

Type of Account : Current Account 

PAN Number : AABCF3718N

Name as on PAN Card  : Fortis Hospitals Limited 

 

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