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Genetic Testing for Personalized Treatment: Patient Guide


Genetic testing is transforming the way doctors diagnose and treat diseases. By analyzing a patient’s DNA, doctors can identify genetic conditions, predict disease risks, and tailor treatments to individual needs. This personalized approach, known as precision medicine, ensures that patients receive the most effective treatments with minimal side effects. In this guide, we’ll explore what genetic testing is, why it matters, how it helps doctors choose the best treatment, and what patients should know before considering it.

Understanding Genetic Testing

What is Genetic Testing?
Genetic testing is a medical test that examines a person’s DNA to identify changes or mutations in genes, chromosomes, or proteins. These tests help diagnose genetic disorders, determine disease risks, and guide doctors in choosing the best treatment.

How Does Genetic Testing Work?
Sample Collection: A sample is taken from blood, saliva, or tissue.
DNA Analysis: Scientists analyze the DNA to detect genetic mutations or variations.
Results Interpretation: A genetic counselor or doctor explains the results and their implications.

Types of Genetic Tests

Why is Genetic Testing Important?

How Genetic Testing Helps in Treatment Selection

Expert Insights: Dr. Shweta Bansal

Dr. Shweta Bansal is a renowned Pediatric Hemato-Oncologist and Bone Marrow Transplant Specialist based in Mumbai. As the Head of Department and Senior Consultant at Sir H. N. Reliance Foundation Hospital, she specializes in treating pediatric hematologic disorders and cancers.

Dr. Bansal completed her postgraduate studies in Pediatrics at Sir Ganga Ram Hospital, Delhi, and trained in Pediatric Hemato-Oncology at Rajiv Gandhi Cancer Hospital, Delhi, and Tata Memorial Hospital, Mumbai. She further advanced her expertise through international fellowships, including St. Jude Children’s Hospital, USA, and NUH, Singapore, focusing on bone marrow transplantation and cutting-edge cancer therapies.

Specialties:
Pediatric Hematology (Anemia, Thalassemia, Aplastic Anemia, Hereditary Blood Disorders)
Platelet Disorders, Bleeding Disorders, Immunodeficiency Disorders
Pediatric Oncology (Leukemia, Lymphoma, Brain Tumors, Sarcoma, Wilms' Tumor, Neuroblastoma)
Precision Oncology, Immunotherapy, Bone Marrow Transplantation

For consultations, visit Sir H. N. Reliance Foundation Hospital, Prarthana Samaj, Raja Ram Mohan Roy Rd, Girgaon, Mumbai, Maharashtra 400004.

FAQs About Genetic Testing

No, it typically involves a simple blood draw or saliva sample.

Not always. It identifies risks and mutations but doesn't always confirm a disease.

Results can take from a few days to several weeks, depending on the test.

Costs vary, but many tests are covered by insurance if deemed medically necessary.

No, it can indicate risk for many conditions but not guarantee their development.

It's most beneficial for those with a family history of genetic disorders or who need personalized treatment options.

Most tests are highly accurate, but interpretation should be done by a qualified genetic counselor or doctor.

Consult your doctor to discuss preventive measures, lifestyle changes, and treatment options.

Conclusion