Panacea’s Post

👨👩👦 Knowing your family medical history is of the utmost importance for any hereditary condition. The '3-2-1 criteria' is used to assess risk before genetic testing. That's where the patient meets the following: 3️⃣ - Three or more relatives diagnosed with a Lynch-associated cancer 2️⃣ - At least two consecutive generations affected 1️⃣ - At least one of those relatives was diagnosed with a Lynch-associated cancer before the age of 50 Lynch syndrome is inherited from one parent that passes on a gene mutation. It is possible to inherit Lynch-related gene mutations from both parents, much like author Sam Rose who was diagnosed with Continual Mismatch Repair Deficiency, or 'double Lynch syndrome' as she described it. #LynchSyndrome #familyhistory #healthawareness #genetics #cancerprevention

SpCas9 has revolutionized modern medicine with groundbreaking potential for treating genetic diseases, cancer, and infectious diseases. However, as scientists push the boundaries of gene editing, it's time to explore beyond SpCas9. Expand your knowledge on the cutting-edge of genetic research and discover how these alternative #crispr nucleases could transform therapeutic applications in our blog. 🔗 👉 https://lnkd.in/dzixA7aA

Did you know that 5-10% of cancers are strongly hereditary, caused by gene mutations passed down through generations? This is why genetic counseling and testing are crucial for families with a cancer history, to identify those at risk and offer early interventions. #WellnessWednesday #PETCT #CancerDetection #HauzKhas #SouthDelhi #PETCTDelhi #PETCTHauzKhas #CancerDelhi #CancerHauzKhas #NuclearMedicne #HealthcareForAll #AffordableCare #DiagnosticImaging #PSMACTScan #EarlyDetection

🎤🎙️ ATTENTION PLEASE 📢📣🔔 🚨🛑 BE ALERT ❗❌ IT IS Possible to know your risks of getting cancer in the next 10, 20 or 30 years! How? Genetic counselors can talk with you about getting some tests that will tell your risk of getting cancer based on your family history and other risk factors. This cancer gene testing will involve them analyzing your genetic material to identify a mutation or variation that could be associated with developing some types of cancer. Get your genetic insights from Utogenx today! Our expert genetic counselors will guide you to understand your genetic landscape and empower you to make informed health decisions. Visit www.utogenx.com today to book an appointment with a genetic counselor on our platform for just 2K or chat with us on WhatsApp: https://lnkd.in/drJTer2b #geneticcounseling #genetictesting #cancer #cancerrisks #cancertesting #familyhistory #healthhistory #genetics #cancerresearch #cancerawareness #cancertreatment #cancersupport #cancerwarrior #healthcare #health #knowyourrisk #knowyourstatus

In this session at #SynBioBeta2024, we will delve into the world of programmable gene and cell therapies, two of the most promising frontiers in #syntheticbiology. Learn about the latest advancements in these fields, and how they are reshaping the landscape of medical treatments for a myriad of diseases, including genetic disorders and cancers: https://lnkd.in/eCVgysZx #genetherapy #celltherapy

New year, new opportunities. For me, that means: 1. more lives that can be impacted by educating about hereditary cancers and how genetic testing can be lifesaving for entire families; 2. more testing funded by My Faulty Gene for people who need testing but do not have access; and 3. reaching untested family members of individuals with a known mutation. This year, I am not going to sell myself short in the impact I can make in the lives of others. This is the year I will find others who share my passion and will join me in making an impact. 2024. This is the year. How about you? What are you going to accomplish this year? #hereditarycancer #genetictesting #familyhealthhistory #knowyourrisk #goals2024 #patientadvocate

As genetic testing is evolving, we need a way to address the frequent medical management changes. In 2022, My Gene Counsel delivered 343 unique notifications electronically to patients and clinicians when tracking 66 hereditary cancer genes. mGC ensures that patients and clinicians receive the most recent and relevant updates based on their genetic information. https://hubs.li/Q028yj9Z0 #PrecisionMedicine #GeneChat

#MedullaryThyroidCancer (MTC) is a rare form of #cancer – but broad-based #GeneticTesting can have a major impact on patient diagnosis and treatment. Ahead of #WorldThyroidDay, refresh your knowledge of one cause of #ThyroidCancer – RET gene mutations – and why timely comprehensive genomic profiling is key. Learn more from the THANC Foundation: https://e.lilly/4aQ4sco

Podcast by NICE on our new guideline [NG241]: Ovarian cancer: identifying and managing familial and genetic risk

𝐔𝐧𝐢𝐭𝐞𝐝 𝐒𝐭𝐚𝐭𝐞𝐬 𝐆𝐞𝐧𝐞𝐭𝐢𝐜 𝐓𝐞𝐬𝐭𝐢𝐧𝐠 𝐌𝐚𝐫𝐤𝐞𝐭 𝐒𝐢𝐳𝐞, 𝐚𝐧𝐝 𝐅𝐨𝐫𝐞𝐜𝐚𝐬𝐭 𝟐𝟎𝟐𝟒-𝟐𝟎𝟑𝟐 The United States genetic testing market size is projected to exhibit a growth rate (CAGR) of 11.80% during 2024-2032. The rapid progress in genomic science and technology, the rising availability of DTC genetic testing kits, and the increasing prevalence of cancer and the recognition of the role of genetics in cancer risk represent some of the key factors driving the market. Read More: https://lnkd.in/gVdah7wN #Size #Share #Trends #Growth #UnitedStatesGeneticTestingMarket