Sickle cell nephropathy

Sickle cell nephropathy is a major complication of sickle cell disease. It manifests in different forms, including glomerulopathy, proteinuria, hematuria, and tubular defects, and frequently results in end-stage renal disease (ESRD). Different pathophysiologic mechanisms have been proposed to explai...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Hariri, Essa (author)
مؤلفون آخرون: Mansour, Anthony (author), El Alam, Andrew (author), Daaboul, Yazan (author), Korjian, Serge (author), Bahous, Sola Aoun (author)
التنسيق: article
منشور في: 2018
الوصول للمادة أونلاين:http://hdl.handle.net/10725/10756
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://link.springer.com/article/10.1007/s11255-018-1803-3
الوسوم: إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
_version_ 1864513487419473920
author Hariri, Essa
author2 Mansour, Anthony
El Alam, Andrew
Daaboul, Yazan
Korjian, Serge
Bahous, Sola Aoun
author2_role author
author
author
author
author
author_facet Hariri, Essa
Mansour, Anthony
El Alam, Andrew
Daaboul, Yazan
Korjian, Serge
Bahous, Sola Aoun
author_role author
dc.creator.none.fl_str_mv Hariri, Essa
Mansour, Anthony
El Alam, Andrew
Daaboul, Yazan
Korjian, Serge
Bahous, Sola Aoun
dc.date.none.fl_str_mv 2018
2019-06-07T10:30:47Z
2019-06-07T10:30:47Z
2019-06-07
dc.identifier.none.fl_str_mv 1573-2584
http://hdl.handle.net/10725/10756
Hariri, E., Mansour, A., El Alam, A., Daaboul, Y., Korjian, S., & Bahous, S. A. (2018). Sickle cell nephropathy: an update on pathophysiology, diagnosis, and treatment. International urology and nephrology, 50(6), 1075-1083.
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://link.springer.com/article/10.1007/s11255-018-1803-3
dc.language.none.fl_str_mv en
dc.relation.none.fl_str_mv International Urology and Nephrology
dc.rights.*.fl_str_mv info:eu-repo/semantics/openAccess
dc.title.none.fl_str_mv Sickle cell nephropathy
an update on pathophysiology, diagnosis, and treatment
dc.type.none.fl_str_mv Article
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
description Sickle cell nephropathy is a major complication of sickle cell disease. It manifests in different forms, including glomerulopathy, proteinuria, hematuria, and tubular defects, and frequently results in end-stage renal disease (ESRD). Different pathophysiologic mechanisms have been proposed to explain the development of nephropathy in SCD, where hemolysis and vascular occlusion are the main contributors in the manifestations of this disease. Markers of renal injury, such as proteinuria and tubular dysfunction, have been associated with outcomes among patients with sickle cell nephropathy and provide means for early detection of nephropathy and screening prior to progression to renal failure. In small-sized clinical trials, hydroxyurea has demonstrated to be effective in slowing the progression to ESRD. Dialysis and renal transplantation represent the last resort for patients with sickle cell nephropathy. Nevertheless, despite the availability of diagnostic and therapeutic strategies, sickle cell nephropathy remains a challenging and under-recognized complication for patients with sickle cell disease.
eu_rights_str_mv openAccess
format article
id LAURepo_8a6f3dd1aae229fa33a48c9f5f11e62b
identifier_str_mv 1573-2584
Hariri, E., Mansour, A., El Alam, A., Daaboul, Y., Korjian, S., & Bahous, S. A. (2018). Sickle cell nephropathy: an update on pathophysiology, diagnosis, and treatment. International urology and nephrology, 50(6), 1075-1083.
language_invalid_str_mv en
network_acronym_str LAURepo
network_name_str Lebanese American University repository
oai_identifier_str oai:laur.lau.edu.lb:10725/10756
publishDate 2018
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
spelling Sickle cell nephropathyan update on pathophysiology, diagnosis, and treatmentHariri, EssaMansour, AnthonyEl Alam, AndrewDaaboul, YazanKorjian, SergeBahous, Sola AounSickle cell nephropathy is a major complication of sickle cell disease. It manifests in different forms, including glomerulopathy, proteinuria, hematuria, and tubular defects, and frequently results in end-stage renal disease (ESRD). Different pathophysiologic mechanisms have been proposed to explain the development of nephropathy in SCD, where hemolysis and vascular occlusion are the main contributors in the manifestations of this disease. Markers of renal injury, such as proteinuria and tubular dysfunction, have been associated with outcomes among patients with sickle cell nephropathy and provide means for early detection of nephropathy and screening prior to progression to renal failure. In small-sized clinical trials, hydroxyurea has demonstrated to be effective in slowing the progression to ESRD. Dialysis and renal transplantation represent the last resort for patients with sickle cell nephropathy. Nevertheless, despite the availability of diagnostic and therapeutic strategies, sickle cell nephropathy remains a challenging and under-recognized complication for patients with sickle cell disease.PublishedN/A2019-06-07T10:30:47Z2019-06-07T10:30:47Z20182019-06-07Articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1573-2584http://hdl.handle.net/10725/10756Hariri, E., Mansour, A., El Alam, A., Daaboul, Y., Korjian, S., & Bahous, S. A. (2018). Sickle cell nephropathy: an update on pathophysiology, diagnosis, and treatment. International urology and nephrology, 50(6), 1075-1083.http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.phphttps://link.springer.com/article/10.1007/s11255-018-1803-3enInternational Urology and Nephrologyinfo:eu-repo/semantics/openAccessoai:laur.lau.edu.lb:10725/107562021-03-19T10:45:23Z
spellingShingle Sickle cell nephropathy
Hariri, Essa
status_str publishedVersion
title Sickle cell nephropathy
title_full Sickle cell nephropathy
title_fullStr Sickle cell nephropathy
title_full_unstemmed Sickle cell nephropathy
title_short Sickle cell nephropathy
title_sort Sickle cell nephropathy
url http://hdl.handle.net/10725/10756
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://link.springer.com/article/10.1007/s11255-018-1803-3