How is Congenital Myastenic Syndrome (CMS) Different from Myasthenia Gravis (MG)? 💭 🔗 Get the basics about CMS, a rare genetic condition: https://lnkd.in/grFN-58i - #CongenitalMyasthenicSyndrome #CMS #MyastheniaGravis #MG #raredisease #rarediseases #rarediseaseawareness #KnowRare
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Hereditary Hemorrhagic Telangiectasia (HHT) is a genetic bleeding disorder that can seriously impact a patient’s quality of life. Learn more about this condition from Troy Woodard MD FACS, as well as our personalized approach to care. #HHT #Rhinology
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World Retinitis Pigmentosa Day raises awareness about a group of genetic disorders that cause retinal degeneration and vision loss. This day promotes education, support, and research to improve the lives of those affected by this condition, aiming for early diagnosis and potential treatments. #WorldRPDay, #RetinitisPigmentosa, #VisionLoss, #RPawareness, #SupportRP, #GeneticDisorders, #EyeHealth, #RPResearch, #BlindnessAwareness
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Breaking down #PFIC: progressive familial intrahepatic cholestasis (PFIC) is a rare genetic disorder caused by defects in genes that proteins need to form bile and transport it out of the liver. This rare disorder affects 1 in every 50,000 to 100,000 births in the US and Europe. To learn more, visit https://bit.ly/40F5cNq
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#PolycysticKidneyDisease (PKD) is a genetic condition causing fluid-filled cysts in kidneys. Early detection is key! Consult our kidney specialists: www.kailashhealthcare.com #baatsehatki #kidneydisease #PKD #Cystickidneydisease
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July is National Hemochromatosis Screening & Awareness Month! Hereditary (or inherited) hemochromatosis is one of the most common genetic conditions in the U.S., and can be passed down in a family through different inheritance patterns. 👩⚕️ Hemochromatosis leads to high iron levels in the body that can cause organ and tissue damage. Early detection is important to ensure treatment is started in time to prevent such damage. 🧬 If you have a family history of hemochromatosis, you and your family members have a higher chance of having this condition and are recommended to talk with your providers about hemochromatosis screening. You may also benefit from talking with a genetic counselor to discuss hereditary forms of this condition by visiting https://lnkd.in/gPY5uT3! #HemochromatosisAwareness #HereditaryHemochromatosis
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Understanding Thalassemia is key to managing it effectively. Explore our FAQ carousel to learn more about this genetic condition and the importance of early detection. Let us spread awareness together. #ThalassemiaAwareness #Thalassemia #thalassemia #thalassemiafreeindia #GeneticHealth #genetichealth #genetichealthtested #genetichealthtesting #VaidyaHealthInsights #Thane #Mumbai #DrVaidya #HealthAwareness #MumbaiHealth #AarogyaVaidyaLab #drvaidyaslaboratory #drvaidyaslab #DrVaidya #drvaidyas
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Marfan Syndrome Awareness Month Marfan syndrome is a genetic condition that affects the body’s connective tissue which holds all the body’s cells, organs and tissue together. #marfansyndromeawarenessmonth #PrismMarketView #PrismMediaWire #PrismDigitalMedia
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Sudden cardiac death in athletes is a rare yet serious challenge, often linked to undetected cardiovascular issues. Genetic screening plays a vital role in identifying specific risks associated with these conditions, as each can vary greatly. Follow us to know more... #HeartHealth #GeneticScreening #SuddenCardiacDeath #AthleteWellness #healthString by www.sugarstrings.ai
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📰Published by Blood®, this study analyzed humans & 🐭with genetic FXIII-A deficiency. Findings demonstrated that clotting factor XIII A & B subunits are made in different cells, but find & stabilize each other in🩸 Read➡️https://lnkd.in/eVzwEZBK #blood #coagulation #bloodclots
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