Late-onset retinal oxalosis in primary hyperoxaluria type 2 [PDF]
American Journal of Ophthalmology Case ReportsPurpose: To report a previously undescribed case of late-onset vision loss due to retinal oxalosis in a patient with primary hyperoxaluria type 2 (PH2).
Rupak Bhuyan +2 more
exaly +4 more sources
Palmar papules as a manifestation of cutaneous oxalosis in primary hyperoxaluria: A case report and review of the literature [PDF]
Clinical Case Reports (discontinued)Key Clinical Message Cutaneous oxalosis is a rare manifestation of systemic oxalosis, typically associated with primary or secondary hyperoxaluria. We present a rare case of a 23‐year‐old female diagnosed with primary hyperoxaluria and end‐stage renal ...
Thaer Douri, Hadi Alabdullah
exaly +3 more sources
Pathology of Free-Living Loggerhead Turtle (Caretta caretta) Embryos on the Island of Linosa (Italy) [PDF]
Veterinary SciencesOn the beach of Linosa Island (Italy), 43 loggerhead sea turtle (Caretta caretta) unhatched eggs were recovered from nests, formalin-fixed and necropsied.
Frine Eleonora Scaglione +11 more
doaj +2 more sources
Catastrophic retinal vascular occlusion and vision loss due to crystal deposition in end-stage kidney disease treated with peritoneal dialysis [PDF]
American Journal of Ophthalmology Case ReportsPurpose: To report two cases of catastrophic retinal vascular occlusion and crystalline retinopathy due to presumed oxalosis and hyperphosphatemia.
Delu Song +7 more
doaj +2 more sources
Multimodal Imaging Findings Associated With Cardiac Oxalosis Cardiomyopathy
JACC: Case ReportsWe report the case of a 50-year-old woman with secondary oxalosis following bowel resection resulting in restrictive cardiomyopathy and a diagnosis of cardiac amyloidosis based on the initial workup.
Choudhary Anwar Ahmed Chahal +1 more
exaly +3 more sources
Primary hyperoxaluria type I diagnosed after a kidney transplant presenting with subcutaneous calcification: a case report of sodium thiosulfate treatment [PDF]
Frontiers in PharmacologyPrimary hyperoxaluria (PH) is a rare autosomal recessive disorder that results from the overproduction of endogenous oxalate. The diagnosis of PH is often delayed or missed owing to its rarity, variable clinical expression and other diagnostic challenges.
Min Wu +7 more
doaj +2 more sources
Cutaneous oxalosis mimicking calcinosis cutis in a patient on peritoneal dialysis
JAAD Case Reports, 2021 Travis Vandergriff +2 more
exaly +3 more sources
Determinants and impact of calcium oxalate crystal deposition on renal outcomes in acute kidney injury patients [PDF]
Renal FailureObjectives Calcium oxalate (CaOx) crystal deposition in acute kidney injury (AKI) patients is under recognized but impacts renal outcomes. This study investigates its determinants and effects.Methods We studied 814 AKI patients with native kidney ...
Weiwei Yang +5 more
doaj +2 more sources
Journal of Synchrotron Radiation, 2022 Renal oxalosis is a rare cause of renal failure whose diagnosis can be challenging. Synchrotron deep ultraviolet (UV) fluorescence was assayed to improve oxalosis detection on kidney biopsies spatial resolution and sensitivity compared with the Fourier ...
Emmanuel Estève +11 more
doaj +1 more source