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Sickle Cell Disease and the Kidney: Filters Gone Awry.
Lebensburger, Jeffrey D; Derebail, Vimal K.
Afiliação
  • Lebensburger JD; Division of Pediatric Hematology-Oncology, Department of Pediatrics, University of Alabama at Birmingham, 1600 7th Avenue South, Lowder 512, Birmingham, AL 35233, USA.
  • Derebail VK; Division of Nephrology and Hypertension, Department of Medicine, University of North Carolina at Chapel Hill, UNC Kidney Center, 7024 Burnett-Womack, CB 7155, Chapel Hill, NC 27599, USA. Electronic address: vimal_derebail@med.unc.edu.
Hematol Oncol Clin North Am ; 36(6): 1239-1254, 2022 12.
Article em En | MEDLINE | ID: mdl-36400541
Throughout the lifespan, the kidney of a person with sickle cell disease is at increased risk of injury to the glomeruli, tubules, and renal vasculature. This injury manifests as urine concentrating defects, enuresis, albuminuria, acute kidney injury, chronic kidney disease, and end-stage kidney disease. The outcomes for patients who progress to end-stage kidney disease are poor and access to organ transplantation is limited. Therefore, identifying risk factors for progression, intervening with renoprotective agents early in life, and improving access to care are vital for sickle cell patients.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Injúria Renal Aguda / Anemia Falciforme / Falência Renal Crônica Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Injúria Renal Aguda / Anemia Falciforme / Falência Renal Crônica Idioma: En Ano de publicação: 2022 Tipo de documento: Article