7: Fragile X Syndrome And Myotonic Dystrophy : USMLE Step 1 Pathology

📌 𝐅𝐨𝐥𝐥𝐨𝐰 𝐨𝐧 𝐈𝐧𝐬𝐭𝐚𝐠𝐫𝐚𝐦:-   / drgbhanuprakash  
📌𝗝𝗼𝗶𝗻 𝗢𝘂𝗿 𝗧𝗲𝗹𝗲𝗴𝗿𝗮𝗺 𝗖𝗵𝗮𝗻𝗻𝗲𝗹 𝗛𝗲𝗿𝗲:- https://t.me/bhanuprakashdr
📌𝗦𝘂𝗯𝘀𝗰𝗿𝗶𝗯𝗲 𝗧𝗼 𝗠𝘆 𝗠𝗮𝗶𝗹𝗶𝗻𝗴 𝗟𝗶𝘀𝘁:- https://linktr.ee/DrGBhanuprakash

7: Fragile X Syndrome And Myotonic Dystrophy : USMLE Step 1 Pathology

🔬 Join us on a captivating journey through Fragile X syndrome and Myotonic Dystrophy in our specialized Pathology video tailored for USMLE Step 1 preparation! 🌟 These genetic disorders offer unique insights into the molecular mechanisms underlying neurodevelopmental and neuromuscular conditions. 🧬 Fragile X syndrome, the most common inherited form of intellectual disability, results from a CGG repeat expansion in the FMR1 gene, leading to impaired synaptic function and cognitive deficits. 🧠 Myotonic Dystrophy, on the other hand, is a multisystem disorder characterized by CTG repeat expansion in the DMPK gene, causing myotonia, muscle weakness, cardiac abnormalities, and cognitive impairment. 💡 Through comprehensive discussions and clinical correlations, we unravel the pathophysiology, clinical manifestations, diagnostic criteria, and management strategies for Fragile X syndrome and Myotonic Dystrophy, empowering medical students to tackle USMLE Step 1 questions with confidence. 📚 Join us as we delve into the complexities of these genetic disorders, equipping you with the knowledge and skills essential for success in your medical exams and clinical practice!

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