Results 1 to 10 of about 2,344 (196)
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 ...
Hadi Alabdullah, Thaer Douri
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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).
Christie P Thomas +2 more
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Bone marrow oxalosis: An unusual cause of cytopenia in end-stage renal disease; report of two cases
Indian Journal of Pathology and Microbiology, 2018 Systemic oxalosis can be either primary or secondary hyperoxaluria. Oxalosis is a phenomenon in which calcium oxalate crystals deposit in various visceral organs leading to bone marrow (BM) failure and recurrent renal stones.
Seema Sharma +3 more
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Renal Failure, 2021 Objects This study aimed to analyze the clinicopathological features of acute kidney disease (AKD) with renal oxalosis. Methods Data for biopsy-proven AKD with oxalosis diagnosed from Jan 2011 to Oct 2018 was collected.
Tao Su
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Cutaneous oxalosis mimicking calcinosis cutis in a patient on peritoneal dialysis
JAAD Case Reports, 2021 Audrey Rutherford +2 more
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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
Frontiers in Medicine, 2021 Background: Primary hyperoxaluria type 1 (PH1) is a rare monogenic disorder characterized by excessive hepatic production of oxalate leading to recurrent nephrolithiasis, nephrocalcinosis, and progressive kidney damage, often requiring renal replacement ...
David J. Sas +14 more
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JIMD Reports, 2021 Primary hyperoxaluria (PH) is a group of diseases due to mutations in genes coding for enzymes involved in oxalate metabolism. Three types of PH are identified depending on the gene mutated.
Matthieu Halfon +7 more
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Kaleidoscopic Views in the Bone Marrow: Oxalate Crystals in a Patient Presenting with Bicytopenia
Turkish Journal of Hematology, 2016 Pancytopenia associated with BM infiltration of different deposits is a rare condition mostly associated with amyloidosis or the accumulation of iron. One of the rarest deposits in the BM is oxalate crystals due to hyperoxaluria [1,2,3].
Yelda Dere +6 more
doaj +2 more sources