Tag: #PolycysticKidneyDisease
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Potter Syndrome A Rare Forensic Insight into Fetal Renal Anomalies
Introduction: Potter Syndrome, a rare and fatal condition linked to severe renal abnormalities in fetuses, presents both clinical and forensic challenges. This case study investigates the pathological outcomes of a stillborn male fetus diagnosed with Potter Syndrome, offering significant insights into the condition’s origins, diagnostics, and morphological impacts.Visit https://www.forensicscijournal.com/ for more groundbreaking research in forensic…
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Successful Long-Term Tolvaptan Therapy in a Patient with Enlarged Polycystic Kidneys A Case Study
Introduction Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a progressive condition characterized by the enlargement of cystic kidneys and declining renal function. Tolvaptan, a vasopressin V2 receptor antagonist, is widely used to slow this progression. This case study examines an ADPKD patient with significantly enlarged kidneys who responded positively to long-term Tolvaptan therapy. Visit HSPIOA…
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