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.
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