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7728 search results for:

Polycystic Kidney Disease 

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  1. Open Access 08-05-2024 | Aneurysm | Online First

    Aneurysms of splenic artery in a patient with autosomal dominant polycystic kidney disease

  2. 17-01-2024 | Polycystic Kidney Disease | OriginalPaper

    Use of a donor kidney with known autosomal dominant polycystic kidney disease in a highly sensitised paediatric recipient

    We report the use of an autosomal-dominant polycystic kidney disease (ADPKD) donor kidney in a paediatric recipient. A 14-year-old boy on haemodialysis for 4 years following loss of a first kidney transplant, highly sensitised, and with limited …

  3. 13-11-2023 | Chronic Kidney Disease | Letter

    Tubular changes in autosomal dominant polycystic kidney disease patients: observational study

  4. 08-04-2024 | Infertility | Online First

    Secondary infertility due to necrospermia in men with autosomal-dominant polycystic kidney disease: a report of two cases

    Autosomal-dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disease characterized by the formation of numerous cysts in organs other than the kidneys. Although female patients with ADPKD do not have direct fertility …

  5. Open Access 21-03-2024 | Nephrectomy | Online First

    Native nephrectomy in polycystic kidney disease patients on transplant lists: how and when?

    Autosomal dominant polycystic kidney disease (ADPKD), the most common hereditary kidney disease, accounts for approximately 10% of the patients on kidney transplantation waitlists. High rates of complications including hemorrhage, infections …

  6. Open Access 01-12-2024 | Chronic Kidney Disease | OriginalPaper

    Mortality risk in patients with autosomal dominant polycystic kidney disease

    Autosomal dominant polycystic kidney disease (ADPKD) is a dominantly inherited systemic disease characterized by uncontrolled development and growth of multiple renal cysts that lead to gradual enlargement of the kidneys [ 1 ]. Over time, ADPKD …

  7. 23-03-2024 | COVID-19 Vaccination | Online First

    De novo posttransplant membranous nephropathy after COVID-19 vaccination 9 years after renal transplantation in a patient with polycystic kidney disease

    A 63-year-old man with polycystic kidney disease underwent kidney transplantation from his wife. Nine years later, after the first and second doses of the COVID-19 vaccination, he developed proteinuria, hematuria, and elevated C-reactive protein.

  8. 02-03-2024 | Polycystic Kidney Disease | Letter

    Tolvaptan Treatment and Long-Term Impact on Quality of Life in Autosomal Dominant Polycystic Kidney Disease Patients: A Pilot Study

  9. Open Access 01-12-2024 | Polycystic Kidney Disease | OriginalPaper

    Autosomal dominant polycystic kidney disease with ectopic unilateral multicystic kidney: a case report

    Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disorder and the fourth cause of death of end-stage renal disease. The disease has a prevalence of 1:400–1:1000 accounting for 10% of patients on dialysis [ 1 …

  10. Open Access 13-12-2023 | Polycystic Kidney Disease | OriginalPaper

    Estimating risk of rapid disease progression in pediatric patients with autosomal dominant polycystic kidney disease: a randomized trial of tolvaptan

    Autosomal dominant polycystic kidney disease (ADPKD) has historically been considered as an adult disease [ 1 ]. Rates of cyst progression leading to chronic kidney disease are highly variable, however, with approximately 3% of children who carry …

  11. Open Access 01-03-2024 | Polycystic Kidney Disease | Online First

    Elevated hemoglobin levels in renal transplant recipients with polycystic kidney disease versus other etiologies: exploring mechanisms and implications for outcomes

    Polycystic kidney disease is an inherited disorder characterized by the progressive formation of fluid-filled cysts that gradually replace normal kidney tissue. It is one of the main causes of end-stage kidney disease (ESKD), often requiring …

  12. 05-02-2024 | Intracranial Aneurysm | Online First

    Factors associated with early-onset intracranial aneurysms in patients with autosomal dominant polycystic kidney disease

    Intracranial aneurysms and subsequent aneurysmal subarachnoid hemorrhage are serious medical conditions that can be life-threatening. These conditions impose a significant health burden on society due to their relatively younger age of onset …

  13. Open Access 01-12-2024 | Hydrochlorothiazide | OriginalPaper

    HYDROchlorothiazide versus placebo to PROTECT polycystic kidney disease patients and improve their quality of life: study protocol and rationale for the HYDRO-PROTECT randomized controlled trial

    Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and leads to progressive renal cyst formation, to loss of renal function, and frequently to kidney failure [ 1 – 3 ]. In the majority of patients …

  14. 23-01-2024 | Polycystic Kidney Disease | Online First

    Epidemiology and outcomes of pediatric autosomal recessive polycystic kidney disease in the Middle East and North Africa

    The incidence of rare diseases is expected to be comparatively higher in the Middle East and North Africa (MENA) region than in other parts of the world, attributed to the high prevalence of consanguinity. Most MENA countries share social and …

  15. 04-11-2023 | Polycystic Kidney Disease | Erratum

    Correction to: Public support for patients with intractable diseases in Japan: impact on clinical indicators from nationwide registries in patients with autosomal dominant polycystic kidney disease

  16. Open Access 01-12-2023 | Dyslipidemia | OriginalPaper

    Cardiometabolic comorbidities in autosomal dominant polycystic kidney disease: a 16-year retrospective cohort study

    Autosomal-dominant polycystic kidney disease (ADPKD) is the most prevalent hereditary kidney disease [ 1 ] (1:500 to 1:1000) and the fourth most common cause of the end-stage renal disease (ESRD) [ 2 ], which affects over 12 million individuals …

  17. 10-05-2023 | Hepatic Encephalopathy | OriginalPaper

    Fatal acute portal vein thrombosis associated with hepatic cysts in a patient with autosomal dominant polycystic kidney disease

    Autosomal dominant polycystic kidney disease (ADPKD) often involves polycystic liver disease (PLD). In severe cases, PLD can develop various complications. However, fatal acute portal vein thrombosis (APVT) associated with PLD has not been …

  18. 25-10-2023 | Peritoneal Dialysis | Online First

    Complications and prognosis of patients diagnosed with autosomal recessive polycystic kidney disease in neonatal period

    There are no clinical guidelines for performing nephrectomy in patients with autosomal recessive polycystic kidney disease (ARPKD). Few reports have described the clinical course of ARPKD diagnosed in the neonatal period in detail. Here, we report …

  19. Open Access 01-12-2023 | Polycystic Kidney Disease | OriginalPaper

    Co-design of a question prompt list about pregnancy and childbearing for women with polycystic kidney disease: an exploratory sequential mixed-methods study

    Polycystic kidney disease (PKD) is a common genetic disorder that affects up to one in 1,000 people [ 1 – 3 ]. There are two types of PKD: autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease

  20. Open Access 01-12-2023 | Nephrectomy | OriginalPaper

    Shift from severe hypotension to salt-dependent hypertension in a child with autosomal recessive polycystic kidney disease after bilateral nephrectomies: a case report

    Autosomal recessive polycystic kidney disease (ARPKD) is a significant cause of morbidity and mortality in infants and children. The phenotype of ARPKD can be very variable ranging from antenatal kidney function impairment to preservation of …

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