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Pink urine syndrome in an anuric patient during continuous renal replacement therapy: A case report.
Medicine (Baltimore)
August 2024
Réanimation Polyvalente, Centre Hospitalier Universitaire Felix Guyon La Réunion, Saint Denis, France.
Introduction: Pink urine syndrome is a rare, poorly understood condition, often prompted by obesity, insulin resistance, and the drug propofol. It is characterized by pink urine or urine sediment and occurs in the absence of a heme or food-based pigment. The pathophysiology of this syndrome is not yet fully understood but is linked to a uric acid metabolism disorder.
View Article and Find Full Text PDFA Rare Sparkle: A Case of Calcified Kidneys in a Young Infant With Renal Failure.
Cureus
October 2023
Department of Pathology, All India Institute of Medical Sciences, Jodhpur, Jodhpur, IND.
Primary hyperoxaluria-1 (PH1) is an autosomal recessively inherited rare genetic condition due to the deficiency of the hepatic enzyme alanine:glyoxylate aminotransferase which leads to high systemic levels of oxalate and subsequently, early end-stage renal disease and death. Here, we present a case of a three-month-old male infant who presented with loose stools, reduced oral intake, and decreased activity for 12-13 days along with edema and a peeling rash on cheeks, lips, and genitalia. During the entire duration of the inpatient stay, the child was oligoanuric.
View Article and Find Full Text PDFA rare cause of oligoanuric kidney failure - a diagnosis not to miss: Answers.
Pediatr Nephrol
September 2022
Divison of Pediatric Nephrology, Children's Mercy Hospital, 2401 Gillham Road, Kansas City, MO, 64108, USA.
A rare cause of oligoanuric kidney failure - a diagnosis not to miss: Questions.
Pediatr Nephrol
September 2022
Divison of Pediatric Nephrology, Children's Mercy Hospital, 2401 Gillham Road, Kansas City, MO, 64108, USA.
Uncommon Presentation of Atypical Hemolytic Uremic Syndrome: A Case Report.
Indian J Nephrol
April 2021
Department of Pediatric Nephrology, Hospital Vall d'Hebron, Universidad Autónoma de Barcelona, Passeig de la Vall d'Hebron 119, Barcelona, España, Argentina.
Atypical hemolytic uremic syndrome (aHUS) is an ultra-rare disease characterized by microangiopathic hemolytic anemia, thrombocytopenia and renal damage. Its presentation as nephrotic syndrome (NS) during first year of life is uncommon; we describe a child with clinical and laboratory findings of NS whose renal biopsy revealed thrombotic microangiopathy (TMA). A previously healthy 4-month-old male was admitted with severe dehydration, diarrhea and anuria.
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