According to ICMR, 1 in 9 women in India is at risk of developing breast cancer. Breast cancer can be prevented through early screening like self-breast examination, mammography and genetic testing. With rapid advancements in medical genomics, genetic testing aids in the early diagnosis and prevention of breast cancer.
Genetic Counselling and Testing for Breast Cancer Read More »
OncoRx Genomic testing for efficient cancer treatment & management
Offering world’s most trusted comprehensive genomic profiling test with in-depth insights on patients’ clinically relevant biomarkers and genomic alterations matching with FDA approved targeted therapies and immunotherapies.
OncoRx Comprehensive Read More »
What is Pharmacogenomics (PGX) ?
Utilizes whole exome test customized to meet the specific requirements of doctors. We convert the complex genomic information into clinical insights to help prescribe the right medications.
Pharmacogenomics (PGX) Read More »
What is GenepoweRx Total ?
GenepoweRx Total is your DNA/genetic testing that can identify your risk for developing a certain disease condition or passing on a genetic disorder. The medical test offers precise treatment plan and a personalized well-being plan.
Women bring unique perspectives to research and scientific conversation. Gender diversity can have a number of advantages in research in both the academic and private sectors. This Women’s Day let’s pay homage to all the women in science who played significant roles and contributed to the welfare of society.
Women in Science: Doctors who changed the face of Indian Medicine Read More »
Three siblings, two females and one male aged between 40 to 50 years were recommended cancer risk screening, using genomics, by their physician. They have a strong family history of cancer. At present, their father is undergoing treatment for stage 4 pancreatic cancer. Their mother has a history of breast cancer, treated, currently in remission.
Patient Story: Genomic Analysis for Cancer Risk Screening Read More »
Storyline: Paa discusses genetic condition, Progeria aka Hutchinson-Gilford syndrome. This syndrome involves a single gene mutation in lamin A (LMNA) gene necessary for holding the centre of a cell together. It is an extremely rare and progressive disorder seen in children that causes accelerated aging, starting in their first two years of life.
Paa (2009) – based on PROGERIA disorder Read More »
Genomics India Conference 2023 (GIC 2023) held at the NIMHANS convention center, Bengaluru is aligned with the 20th year of the completion of the Human Genome Project, and Genotypic’s 25th year of inception. Around 50 speakers and more than 500 participants from 7 countries attended the GIC 2023.
Statins lower the level of low-density lipoprotein (LDL) cholesterol in the blood, and though generally well-tolerated, they can lead to immune-mediated necrotizing myopathy in a minority of patients.
Statin-induced immune-mediated necrotizing myopathy (IMNM), is an inflammatory myopathy that is a rare complication caused due to statin use.
Statin-triggered immune-mediated necrotizing myopathy Read More »
About 1 in 700 babies are born with Down syndrome (Trisomy 21), a genetic condition that causes intellectual disability. When an infant is born with an extra copy of chromosome 21, it causes distinctive physical features, an elevated risk of health problems like thyroid or heart disease, and intellectual impairments.
Restoring Gonadotropin hormone improves cognition in Down syndrome Read More »
A brand name of Uppaluri K&H Personalized Medicine Clinic Private Limited.
Cracking the ‘One Size Fits All’ theory of medical science while inculcating the philosophy of “You are unique, and so should your medical treatment…”
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