In today’s #readoftheweek📚, learn how lifestyle factors associate with chronic liver disease and if these associations differ based on underlying cardiometabolic perturbations or genetic predisposition. Read this JHEP Reports article: https://lnkd.in/evqKveAx 🙏 to authors Isabel Drake, Alice Giontella, Mariam Miari, Kristina Önnerhag, and Marju Orho-Melander. Lund University Skånes universitetssjukhus (Skåne University Hospital)
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Exciting Update! As we conclude our 'Spotlight Disease of the week' series for Endocrine Disorder Panel, we've explored a spectrum of 17+ diseases, unraveling their intricacies, including conditions like Congenital Adrenal Hyperplasia, Hypogonadotropic Hypogonadism, and more. Our journey into the genetic landscape has unveiled insights into 45+ critical genes, featuring MEN1, CDKN1B, and others. Stay tuned for additional genetic revelations in our upcoming series! Next Up: Renal Panel! Stay tuned for insightful explorations into the world of kidney health! #EndocrineDisorder #RenalDisorder #RenalPanel #SpotlightDiseaseoftheWeek #JourneyintoGeneExploration #StayTuned
What causes the immune system to attack its own body in Type 1 Diabetes? Understanding the interplay of genetics and environment. Type 1 Diabetes is primarily an autoimmune disease where the body's immune system attacks pancreatic cells that produce insulin. Although the exact cause is not fully understood, both genetic predisposition and environmental factors are considered influential. Key insights include: Autoimmune Response: Destruction of insulin-producing cells. #Type1Diabetes #icliniq
TB Research May Transform Inflammatory Disorder Treatments Genetic susceptibility can explain the difference in disease outcomes, said researchers. Read More at: https://lnkd.in/eXknytat #indiareportagenews #headlines #breakingnews #worldnews #indianews #latestnews #Dailyupdates
Did you know millions of people unwittingly endure glaucoma, an invisible cause of vision problems every year? The early symptoms of glaucoma can be hard to diagnose, so people don’t usually find out until it’s too late. Genetic mutations are one of the leading causes of glaucoma, and regular genetic and eye testing can help diagnose it in time, especially for those with a positive family history of the disease. Read on to learn about: ➡️ Glaucoma ➡️ Its genetic risk factors ➡️ Its causes ➡️ How to identify if you’re at risk https://qr.ae/p2RU11 OR https://lnkd.in/djnzb5t3 #glaucoma #eyes #eyecare #eyehealth #vision #visionproblems #geneticmutations #eyetesting #familyhistory #geneticriskfactors #causes #diagnosis #OAG #POAG #JOAG #PCG #ACG #IOP #MYOCgene #CYP1B1gene #LTBP2gene #xcode #xcodelife #genetics #genetest #genetictesting #genetictest #genomics #genome #geneticmakeup #geneticlink #geneticcounseling #genetictraits #genes #DNA #DNAtest #DNAtesting #DNAandhealth #genesandhealth #research #study #findings #nutrition #health #wellness #didyouknow #wednesdaywellness #wednesdaywisdom #wednesdaythoughts #dailypost #dailytips #dailyupdates #everydaylearning
The Link Between Genetics and Gum Disease: Uncovering the Truth Discover how your genes can determine your vulnerability to gum disease and inflammation. Learn about the specific base pair mutations and enzymes that play a role in collagen breakdown. Find out how early markers can help diagnose gum disease before symptoms appear. #GeneticsAndGumDisease #InflammationFactors #CollagenBreakdown #EarlyDiagnosis #DentalHealth #OralHygiene #GumDiseasePrevention #GeneticPredisposition #OralCareTips #DentalWellness
𝗪𝗼𝗻𝗱𝗲𝗿𝗳𝘂𝗹 𝘁𝗼 𝘀𝗲𝗲 𝘁𝗵𝗲 𝗶𝗺𝗽𝗮𝗰𝘁𝗳𝘂𝗹 𝗿𝗲𝘀𝗲𝗮𝗿𝗰𝗵 𝗮𝘁 𝘁𝗵𝗲 𝗩𝗶𝗰𝘁𝗼𝗿 𝗖𝗵𝗮𝗻𝗴 𝗖𝗮𝗿𝗱𝗶𝗮𝗰 𝗥𝗲𝘀𝗲𝗮𝗿𝗰𝗵 𝗜𝗻𝘀𝘁𝗶𝘁𝘂𝘁𝗲! 🌟 Dr. Chai Ann (Andy) Ng is making groundbreaking progress in diagnosing and treating inherited heart disorders using our SyncroPatch 384 system. Their high-throughput genetic test for Long QT Syndrome is revolutionizing the study of genetic variants, delivering faster and more accurate results for patients. Read more about Dr. Ng's story below 👇 #CardiacResearch #GeneticTesting #Arrhythmias #APC #Electrophysiology
Star Scientist Dr Chai Ann (Andy) Ng aims to give patients and families with inherited heart arrhythmias long-hoped-for answers about the cause of their disease. His complex work in our Innovation Centre is helping to improve genetic testing and treatment. Read his story: https://lnkd.in/gUaaa_Th #MedicalResearch #HeartDisease #arrhythmia Jamie Vandenberg
Associate Professor, MUCM |MD( AIIMS, New Delhi); MBBS (Calcutta Medical College)| Member USCAP |Consultant Clinical pathologist;15+ yrs Exp| Winner 🥇: Osmosis Raise The Line Faculty Award 2022 | Founder:@pathology360
The presence of spherocytes doesn’t automatically indicate hereditary spherocytosis because they can also occur in acquired conditions like autoimmune hemolytic anemia, certain infections, or burns. Spherocytes reflect red blood cell membrane damage, which isn’t specific to a single disease. Additional tests, like EMA-binding test or genetic testing, are required to confirm hereditary spherocytosis. #pathology360 #DrKishoreBanerjee.
Research Project Manager chez ERN EpiCARE (European Reference Network for Rare and Complex Epilepsies) & Executive Director of the European Collaboration For Epilepsy Trials
🌻 Join the Genetic Research Study on Sunflower Syndrome! 🌻 We're thrilled to invite you to participate in a genetic research study on Sunflower Syndrome, led by experts Jo Sourbron, Lieven Lagae, Pasquale Striano, and Gerhard Kluger. The goal is to raise awareness about Sunflower Syndrome across Europe, the UK, and beyond, and to uncover its potential genetic underpinnings. 🔍 How You Can Help: If you or someone you care for is affected by Sunflower Syndrome, we kindly ask you to complete a brief questionnaire aimed at evaluating the effectiveness of various medications. Your input is invaluable in advancing our understanding and treatment of this highly stereotyped epilepsy syndrome. 📝 Take the Survey: https://lnkd.in/eXi7YxTT Please share this post and help us spread the word. Together, we can make a difference! #GeneticResearch #SunflowerSyndrome #EpilepsyAwareness #MedicalResearch #HealthcareInnovation ERN EpiCARE - Rare and Complex Epilepsies
Happy #NationalDNADay from all of us at Passage Bio! 🧬 Today we are celebrating all the advancements made in the #geneticmedicine space that have helped pave the way for our vision of delivering life-transforming medicines that can permanently redefine the course of devastating #neurodegenerative diseases. Learn more about our work in genetic medicine: https://loom.ly/hkMUF98
From multiple myeloma to metabolic disorders, hemoglobinopathies, genetic, autoimmune and infectious diseases, Sebia’s portfolio is designed to address clinical needs and improve laboratory efficiency and safety. https://lnkd.in/d4D3udk6 #sebia #sebiaromania #CDT #HbA1c #myeloma
Prof of Global Health, CUNY SPH and Research Professor at ISGlobal, Barcelona, Spain
2moGreat to.see Lund University in the thick of things. I spent a few nice years there completing my Dr Med.