Rupesh Raina, Ahmad Houry, Pratik Rath, Guneive Mangat, Davinder Pandher, Muhammad Islam, Ala'a Grace Khattab, Joseph K Kalout, Sumedha Bagga
Autosomal dominant polycystic kidney disease, also known as ADPKD, is the most common hereditary kidney disease, affecting different age groups. ADPKD can eventually lead to end-stage renal disease. The etiology of ADPKD is genetic, resulting in the formation of cysts containing fluids on the kidneys. Patients with ADPKD present a range of symptoms following a decline in kidney function. Pain, stones, proteinuria and osteoporosis are few of the many symptoms, resulting from decreased kidney function. Tolvaptan, a selective V2 receptor antagonist, is the etiological treatment used for ADPKD...
2022: Drug, Healthcare and Patient Safety