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📌𝐅𝐨𝐥𝐥𝐨𝐰 𝐨𝐧 𝐈𝐧𝐬𝐭𝐚𝐠𝐫𝐚𝐦:- / drgbhanuprakash 📌𝗝𝗼𝗶𝗻 𝗢𝘂𝗿 𝗧𝗲𝗹𝗲𝗴𝗿𝗮𝗺 𝗖𝗵𝗮𝗻𝗻𝗲𝗹 𝗛𝗲𝗿𝗲:- https://t.me/bhanuprakashdr 📌𝗦𝘂𝗯𝘀𝗰𝗿𝗶𝗯𝗲 𝗧𝗼 𝗠𝘆 𝗠𝗮𝗶𝗹𝗶𝗻𝗴 𝗟𝗶𝘀𝘁:- https://linktr.ee/DrGBhanuprakash 🧬 Congenital Adrenal Hyperplasia (CAH) | USMLE Step 1 | 21-Hydroxylase, Salt-Wasting Crisis, Enzyme Map & High-Yield Labs Congenital adrenal hyperplasia (CAH) is a group of inherited genetic disorders that affect the adrenal glands. These disorders cause the adrenal glands to produce an insufficient amount of certain hormones, including cortisol, which can lead to a variety of health problems. CAH is caused by mutations in genes that encode for enzymes involved in the production of cortisol and other hormones in the adrenal glands. The most common type of CAH is caused by a deficiency in the enzyme 21-hydroxylase, which is responsible for converting cholesterol into cortisol. The symptoms of CAH vary depending on the specific type and severity of the disorder, but may include salt wasting, dehydration, low blood pressure, decreased growth, early onset of puberty, and infertility. In severe cases, CAH can cause life-threatening adrenal crises. Treatment for CAH typically involves replacing the deficient hormones with synthetic hormones. This can help to manage symptoms and prevent complications, such as adrenal crises. It is important for individuals with CAH to receive regular medical care and monitoring to ensure that their hormone levels are balanced and that any potential complications are addressed in a timely manner. Individuals with CAH may also benefit from genetic counseling, which can help them understand the risk of passing the disorder on to their children and explore options for family planning. #congenitaladrenalhyperplasia #fmge #fmgevideos #rapidrevisionfmge #fmgejan2023 #mbbslectures #nationalexitexam #nationalexittest #neetpg #usmlepreparation #usmlestep1 #fmge #usmle #drgbhanuprakash #medicalstudents #medicalstudent #medicalcollege #neetpg2023 #usmleprep