Marfan Syndrome: Chromosome 15 Mutation FBN1 Gene #shorts
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FBN1 Fibrillin 1
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FBN1 Fibrillin 1
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FBN1 Fibrillin 1
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FBN1 Fibrillin 1
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SAP FICO S4 HANA FBN1 #sap #sapfico #sapclasses #sapkadapa #saplokesh #learnsap #saptraining
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JuMed on Instagram: "Marfan Syndrome — more than just “being tall.” Marfan is a connective-tissue disorder caused by a mutation in the FBN1 (Fibrillin-1) gene. When fibrillin is faulty, the elastic fibers in your body weaken — and the effects hit multiple systems: 🦴 Skeletal: tall, long limbs, long fingers (arachnodactyly), chest wall deformities 👁️ Eyes: lens dislocation, early myopia ❤️ Heart & Aorta: aortic root dilation, aneurysm risk, mitral valve prolapse — the most serious complications
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