Introduction Mucopolysaccharidoses (MPS) are a group of rare, inherited lysosomal storage disorders caused by the deficiency of enzymes responsible for degrading glycosaminoglycans (GAGs). These conditions result in progressive accumulation of GAGs in tissues, leading to multi-organ dysfunction. While all MPS types share overlapping clinical manife
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ACC, AHA and ESC Recommendations for Heart Failure Management
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Catheter Ablation for Atrial Fibrillation with HF
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Male with Urethral Bleeding due to Insertion of Telephone Wire in Urethra
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