Results 21 to 30 of about 15,419 (219)

Antenatally Diagnosed ADPKD [PDF]

Kidney International Reports, 2018
[Extract] Advances in antenatal ultrasonographyhave substantially improved the counseling of pregnantwomen.1 4With this advancement comes a diagnosticdilemma in the approach to antenatal diagnoses of cystickidney disease. The differential diagnosis of enlargedcystic echogenic kidneys includes autosomal dominantpolycystic kidney disease (ADPKD ...
Aldridge, Melanie, Patel, Chirag, Mallett, Andrew, Trnka, Peter   +3 more
openaire   +3 more sources

Overweight and Obesity and Progression of ADPKD

American Society of Nephrology. Clinical Journal, 2021
Visual Abstract Background and objectives On the basis of earlier observations, we evaluated the association between overweight and obesity and rapid progression of autosomal dominant polycystic kidney disease in participants in the Tolvaptan Efficacy ...
Kristen L. Nowak, C. Steele, Berenice Y. Gitomer, Wenchyi Wang, J. Ouyang, M. Chonchol   +5 more
semanticscholar   +1 more source

Dual Monogenic Cystic Disease Case Report: Autosomal Dominant Polycystic Kidney Disease and Autosomal Dominant Polycystic Liver Disease. [PDF]

Clin Case Rep
ABSTRACT Autosomal dominant polycystic kidney disease (ADPKD) and autosomal dominant polycystic liver disease (ADPLD) are inherited cystic conditions with overlapping features but distinct genetic causes and clinical courses. Here, we report a case of a 50‐year‐old woman with a clinical diagnosis of ADPKD, hypertension, preserved kidney function ...
Brossart AK, Curry K, Punj S, Darwish T, Tabriziani H.   +4 more
europepmc   +2 more sources

Identification of osteopontin as a urinary biomarker for autosomal dominant polycystic kidney disease progression [PDF]

Kidney Research and Clinical Practice, 2022
Background Autosomal dominant polycystic kidney disease (ADPKD), one of the most common human monogenic diseases, is characterized by the presence of numerous fluid-filled renal cysts and is a leading cause of end-stage renal disease (ESRD).
Hyunsuk Kim, Jinmo Sung, Ju Young Bae, Poongyeon Lee, Yun Kyu Oh, Hyunho Kim   +5 more
doaj   +1 more source

Inferior Vena Cava Thrombosis After Nephrectomy of the Native Kidneys in Patients With Autosomal Dominant Polycystic Kidney Disease. [PDF]

IJU Case Rep
ABSTRACT Background Inferior vena cava (IVC) thrombosis associated with autosomal dominant polycystic kidney disease (ADPKD), caused by mechanical compression from a large liver or renal cysts, has previously been reported. However, postoperative thrombosis following nephrectomy of the native kidneys has not been described.
Matsushita Y, Watanabe K, Aoki T, Tsuyuki H, Watanabe H, Tamura K, Katahashi K, Isobe S, Motoyama D, Inamoto T.   +9 more
europepmc   +2 more sources

The Relationship Between Dietary Intakes and Total Kidney Volume in Patients with Autosomal Dominant Polycystic Kidney Disease Dietary Intake and Polycystic Kidney Volume

Haseki Tıp Bülteni, 2022
Aim:There is a need to understand autosomal dominant polycystic kidney disease (ADPKD) patients’ dietary habits since dietary interventions may have potential effects on ADPKD.
Yonca Sevim, Egemen Cebeci, Ozlem Persil Ozkan, Yildiray Savas, Savas Ozturk, Gul Kiziltan   +5 more
doaj   +1 more source

Patients with Protein-Truncating PKD1 Mutations and Mild ADPKD.

American Society of Nephrology. Clinical Journal, 2021
BACKGROUND AND OBJECTIVES Progression of autosomal dominant polycystic kidney disease (ADPKD) is highly variable. On average, protein-truncating PKD1 mutations are associated with the most severe kidney disease among all mutation classes. Here, we report
M. Lanktree, E. Guiard, Pedram Akbari, M. Pourafkari, Ioan-Andrei Iliuta, S. Ahmed, A. Haghighi, N. He, Xuewen Song, A. Paterson, K. Khalili, Y. Pei   +11 more
semanticscholar   +1 more source

Rapidly progressive nephromegaly in a neonate with autosomal recessive poly cystic kidney disease [PDF]

Journal of Nephropathology, 2017
Background: Autosomal recessive polycystic kidney disease (ARPKD) associates with significant renal and liver-related morbidity and mortality in children. Rarely severe enlargement of kidneys necessitates nephrectomy and initiating dialysis.
Mitra Naseri, Nona Zabolinejad, Syed Ali Alamdaran, Reza Shojaeian   +3 more
doaj   +1 more source

Use of the Urine-to-Plasma Urea Ratio to Predict ADPKD Progression.

American Society of Nephrology. Clinical Journal, 2021
BACKGROUND AND OBJECTIVES Predicting disease progression in patients with autosomal dominant polycystic kidney disease (ADPKD) poses a challenge, especially in early-stage disease when kidney function is not yet affected.
Judith E. Heida, R. Gansevoort, A. L. Messchendorp, E. Meijer, N. Casteleijn, W. Boertien, Debbie Zittema   +6 more
semanticscholar   +1 more source

Radiologic and clinical bronchiectasis associated with autosomal dominant polycystic kidney disease. [PDF]

PLoS ONE, 2014
Polycystin 1 and 2, the protein abnormalities associated with autosomal dominant polycystic kidney disease (ADPKD), are also found in airway cilia and smooth muscle cells.
Teng Moua, Ladan Zand, Robert P Hartman, Thomas E Hartman, Dingxin Qin, Tobias Peikert, Qi Qian   +6 more
doaj   +1 more source