Penyakit Ginjal Polikistik disertai Anemia Hemolitik Autoimun

The hereditary forms of polycystic kidney disease autosomal dominant PKD (ADPKD) and recessive (ARPKD) are the main forms. ADPKD is a multifactorial disorder characterized by bilateral renal cysts commonly affects adult patients. most common extrarenal manifestations liver often incidental findings clinically insignificant. A case report has been reported with in kidneys autoimmune hemolytic anemia. progressive symptoms tend to get worse over time. involves managing slowing progression. serious complication end stage failure. This aim this study were determine laboratory tests that confirm diagnosis accompanied