Publication:
Renal Papillary Necrosis as the First Presenting Clinical Feature in a Sickle Beta and Thalassemic Child

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorKumar, Jagadish
dc.contributor.authorChowdary, Satyesh
dc.contributor.authorVG, Manjunath
dc.contributor.authorDas, Sudha Kiran
dc.contributor.authorVuyyuru, Manovihari
dc.date.accessioned2025-12-22T06:36:26Z
dc.date.available2025-12-22T06:36:26Z
dc.date.issued2020
dc.descriptionJagadish Kumar Department of Paediatrics, Jagadguru Sri Shivarathreeshwara Medical College, Jagadguru Sri Shivarathreeshwara University, Mysore, India Satyesh Chowdary Department of Paediatrics, Jagadguru Sri Shivarathreeshwara Medical College, Jagadguru Sri Shivarathreeshwara University, Mysore, India Manjunath VG Department of Paediatrics, Jagadguru Sri Shivarathreeshwara Medical College, Jagadguru Sri Shivarathreeshwara University, Mysore, India Sudha Kiran Das Department of Paediatrics, Jagadguru Sri Shivarathreeshwara Medical College, Jagadguru Sri Shivarathreeshwara University, Mysore, India Manovihari Vuyyuru Department of Paediatrics, Jagadguru Sri Shivarathreeshwara Medical College, Jagadguru Sri Shivarathreeshwara University, Mysore, India
dc.description.abstractAbstract: In sickle cell disease (SCD), the clinical manifestations are due to episodes of vascular occlusion and haemolysis. Most of the children experience vaso-occlusive pain episodes by the age of six years. Renal injury in sickle cell disease referred to as sickle cell nephropathy is a frequent yet under-recognised complication. Renal papillary necrosis (RPN) as the first presentation in SCD is rare. We are reporting a 12 year old child with no prior vaso-occlusive episodes, presenting with renal papillary necrosis due to Sickle Beta and Thalassemia.
dc.identifierhttps://doi.org/10.3126/jnps.v40i3.29617
dc.identifier.urihttps://hdl.handle.net/20.500.14572/3769
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectRenal Papillary Necrosis
dc.subjectSickle Beta and Thalassemia
dc.subjectSickle Cell Disease
dc.subjectSickle Cell Nephropathy
dc.titleRenal Papillary Necrosis as the First Presenting Clinical Feature in a Sickle Beta and Thalassemic Child
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage277
oaire.citation.startPage274
relation.isJournalIssueOfPublication8a626194-2378-44dd-800f-96bb60db9079
relation.isJournalIssueOfPublication.latestForDiscovery8a626194-2378-44dd-800f-96bb60db9079
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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