A Photo Shoot of Proteinuria

Benzing, Thomas

doi:10.1681/asn.2012040395

Journal of the American Society of Nephrology

2012

DOI: 10.1681/asn.2012040395

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A Photo Shoot of Proteinuria

Thomas Benzing

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Cited by 2 publications

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“…And liver transplantation or dialysis is required in treating end-stage renal failure [1][2][3]20,[23][24][25][26] Polycystic kidney disease of both the ADPKD and ARPKD types is a majorcause of end-stage renal failure and a common indication for dialysis or kidney transplantation. The patient becomes suggestive to transplantation or most commonly, dialysis at 70 in 50% of cases.…”

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Supporting Examination of Ct-Scan on Polycystic Kidney Disease Patient at Dustira Hospital Cimahi Indonesia

Fiddyanti,

Alwani

2023

Journal of Health and Dental Sciences

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Polycystic Kidney Disease (PKD) is the growth of many kidney cysts. PKD is divided into Autosomal Dominant Polycystic Kidney Disease (ADPKD) and Autosomal Recessive Polycystic Kidney Disease (ARPKD). ADPKD prevalence 1:500 and ARPKD 1:6000-40000. The patient, a 34-year-old male, came to the hospital with the main complaint of bilateral low back pain. Patients are given symptomatic treatment by diclofenac sodium 50mg 2 dd 1—supporting Examination for PKD diagnosis with CT-Scan. The author is interested in studying more about PKD because it is asymptomatic and only becomes symptomatic at the age of 30-40 years in ADPKD and has high mortality in the ARPKD type.

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confidence: 99%

Supporting Examination of Ct-Scan on Polycystic Kidney Disease Patient at Dustira Hospital Cimahi Indonesia

Fiddyanti,

Alwani

2023

Journal of Health and Dental Sciences

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The role of the podocyte in albumin filtration

2013

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In the past decade, our understanding of the role of podocytes in the function of the glomerular filtration barrier, and of the role of podocyte injury in the pathogenesis of proteinuric kidney disease, has substantially increased. Landmark genetic studies identified mutations in genes expressed by podocytes as a cause of albuminuria and nephrotic syndrome, leading to breakthrough discoveries from many laboratories. These discoveries contributed to a dramatic change in our view of the glomerular filtration barrier of the kidney and of the role of podocyte injury in the development of albuminuria and progressive kidney disease. In the past several years, studies have demonstrated that podocyte injury is a major cause of marked albuminuria and nephrotic syndrome, and have confirmed that podocytes are important for the maintenance of an intact glomerular filtration barrier. An essential role of loss of these cells in the pathogenesis of glomerulosclerosis and progressive proteinuric kidney disease has also been identified. In this Review, we discuss the importance of podocytes for the maintenance of an intact glomerular filtration barrier and their role in albumin handling.

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A Photo Shoot of Proteinuria

Cited by 2 publications

References 30 publications

Supporting Examination of Ct-Scan on Polycystic Kidney Disease Patient at Dustira Hospital Cimahi Indonesia

Supporting Examination of Ct-Scan on Polycystic Kidney Disease Patient at Dustira Hospital Cimahi Indonesia

The role of the podocyte in albumin filtration

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