Publication:
Surgical Management of Autosomal Dominant Polycystic Kidney Disease: Principles and Current Practice

creativeworkseries.issnJNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X
dc.contributor.authorShrestha, Badri Man
dc.date.accessioned2025-09-25T07:06:19Z
dc.date.available2025-09-25T07:06:19Z
dc.date.issued2023
dc.descriptionBadri Man Shrestha Sheffield Kidney Institute, Sheffield Teaching Hospitals NHS Trust, Sheffield, United Kingdom
dc.description.abstractAbstract Autosomal dominant polycystic kidney disease is the third most common cause of renal failure with no definitive treatment available that can directly target the development and growth of the cysts. Endeavours are being made to retard the growth of the cysts and preservation of renal function through medical treatment. However, 50% of the autosomal dominant polycystic kidney disease-affected persons develop complications and end-stage renal disease by the age of fifty-five and need surgical intervention for the management of complications, creation of dialysis access and renal transplantation. This review highlights the principles and current practice pertinent to the surgical management of autosomal dominant polycystic kidney disease.
dc.identifierhttps://doi.org/10.31729/jnma.8159
dc.identifier.urihttps://hdl.handle.net/20.500.14572/2365
dc.language.isoen_US
dc.publisherNepal Medical Association
dc.subjectPolycystic kidney disease
dc.subjectNephrectomy
dc.subjectTransplantation.
dc.titleSurgical Management of Autosomal Dominant Polycystic Kidney Disease: Principles and Current Practice
dc.typeArticle
dspace.entity.typePublication
local.article.typeReview Article
oaire.citation.endPage491
oaire.citation.startPage485
relation.isJournalIssueOfPublication4868a5d2-9d9a-41c1-8965-99b78270b87b
relation.isJournalIssueOfPublication.latestForDiscovery4868a5d2-9d9a-41c1-8965-99b78270b87b
relation.isJournalOfPublicatione6e146a0-0ece-4aba-aa0a-6ccfbd10a12a

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