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- W4308131946 abstract "Autosomal Dominant Polycystic Kidney Disease, known by its acronym ADPKD (Autosomal Dominant Polycystic kidney disease), is a condition of genetic origin characterized by two types of mutations in the PKD1 and PKD2 genes that code for polycystins (PC) 1 and 2, respectively. It is associated with extrarenal manifestations, both cystic and non-cystic; the liver is the most affected organ within the cystic manifestations; as well as cerebral vascular alterations, in non-cystic ones. We report a 44-year-old woman with polycystic hepato-renal disease (PLKD) complicated by intestinal subocclusion." @default.
- W4308131946 created "2022-11-08" @default.
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- W4308131946 date "2022-09-30" @default.
- W4308131946 modified "2023-09-27" @default.
- W4308131946 title "Hepatorenal polychistic disease complicated with intestinal suboclusion: A case report" @default.
- W4308131946 doi "https://doi.org/10.17268/rmt.2022.v17i3.4218" @default.
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