نتایج جستجو برای: autosomal dominant polycystic kidney disease

تعداد نتایج: 1745479  

Journal: :Journal of the American Society of Nephrology 2014

Journal: :Seminars in nephrology 2015
Andrew Mallett Manish Patel David J Tunnicliffe Gopala K Rangan

a. We recommend that unenhanced computed tomography is the preferred imaging modality for the diagnosis of suspected nephrolithiasis in autosomal dominant polycystic kidney disease (1B). b. We recommend that patients with autosomaldominant polycystic kidney disease complicated by nephrolithiasis should be investigated for predisposing urinary metabolic abnormalities (1C) and we suggest receive ...

2012
Toshihiro Misumi Kentaro Ide Takashi Onoe Masataka Banshodani Hirofumi Tazawa Yoshifumi Teraoka Ryuichi Hotta Masahiro Yamashita Hirotaka Tashiro Hideki Ohdan

INTRODUCTION We report an instructive case of incidental renal cell carcinoma in a patient with autosomal dominant polycystic kidney disease who underwent simultaneous bilateral native nephrectomy and living donor renal transplantation. CASE PRESENTATION A 57-year-old Asian man with end-stage kidney disease due to autosomal dominant polycystic kidney disease received a living kidney graft fro...

Journal: :Seminars in nephrology 2015
Gopala K Rangan Vincent W Lee Stephen I Alexander Chirag Patel David J Tunnicliffe Philip Vladica

a. We recommend prior to screening at-risk individuals should receive appropriate counseling regarding the potential benefits and risks of making the diagnosis of autosomal dominant polycystic kidney disease from their general practitioner in consultation with a clinical geneticist or nephrologist (2A). b. We recommend that screening of individuals who are at-risk (50% chance) be performed by r...

Journal: :Seminars in nephrology 2015
Michel Tchan Judy Savige Chirag Patel Andrew Mallett Allison Tong David J Tunnicliffe Gopala K Rangan

a. We recommend that the standard methodology for genetic diagnosis of autosomal dominant polycystic kidney disease is polymerase chain reaction (PCR) amplification (including long-range PCR for the first 33 exons of PKD1) followed by Sanger sequencing (1A) or next-generation sequencing where available (1D). b. We suggest that individuals with a clinical diagnosis of autosomal dominant polycyst...

Journal: :Iranian journal of kidney diseases 2014
Masoumeh Mohkam Shirin Shohadaii Farshid Kompani Hamid Reza Aghadoost Seyed Ali Hojati Nasrin Esfandiar

Tuberous sclerosis complex (TSC) is a multisystemic inherited autosomal dominant disease characterized by the development of hamartomas in the brain and kidneys. In about 2% of patients, polycystic kidney disease is present, which may result in different stages of renal insufficiency. Acute kidney failure has not been reported in infants with TSC. We report a female infant with TSC who was admi...

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