Results 1 to 10 of about 2,169 (151)

Late-onset retinal oxalosis in primary hyperoxaluria type 2 [PDF]

American Journal of Ophthalmology Case Reports
Purpose: 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, Christie Thomas, Timothy M Boyce   +2 more
exaly   +4 more sources

Critically ill, tubular injury, delayed early recovery: characteristics of acute kidney disease with renal oxalosis

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.
Su-Xia Wang, Tao Su, Xiaojuan Yu
exaly   +2 more sources

Systemic Oxalosis Mimicking Transthyretin Amyloid Cardiomyopathy [PDF]

JACC: Case Reports
Background: Technetium-99m pyrophosphate (Tc-99m PYP) scintigraphy is a noninvasive imaging modality in the diagnosis of transthyretin amyloid cardiomyopathy (ATTR-CM), though false positive results may result in adverse clinical outcomes.
Bhavya Ancha, MD, Virginia Hahn, MD, Charles Steenbergen, Jr., MD, PhD, Cheng-Ying Ho, MD, PhD, Ahmad Kohsar, DO, Emily Brown, MGC, CGC, Mark Ranek, PhD, Claire Brookmeyer, MD, Michael Polydefkis, MD, Joban Vaishnav, MD   +9 more
doaj   +2 more sources

Pathology of Free-Living Loggerhead Turtle (Caretta caretta) Embryos on the Island of Linosa (Italy) [PDF]

Veterinary Sciences
On 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, Matteo Cuccato, Erica Longato, Paola Pregel, Daniele Zucca, Stefano Nannarelli, Alessandra De Lucia, Marco Pilia, Elisabetta Manuali, Marco Gobbi, Enrico Bollo, Simonetta Appino   +11 more
doaj   +2 more sources

Palmar papules as a manifestation of cutaneous oxalosis in primary hyperoxaluria: A case report and review of the literature

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   +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 Reports
Purpose: To report two cases of catastrophic retinal vascular occlusion and crystalline retinopathy due to presumed oxalosis and hyperphosphatemia.
Delu Song, Charles Ginsberg, Eric Nudleman, Shyamanga Borooah, Andrew King, Elodie Bousquet, David Sarraf, Michael Goldbaum   +7 more
doaj   +2 more sources

Cutaneous oxalosis mimicking calcinosis cutis in a patient on peritoneal dialysis

JAAD Case Reports, 2021
Travis Vandergriff, Arturo R Dominguez
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 Pharmacology
Primary 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, Jing Lu, Yu-Jia Wang, Yong-Qi Li, Qing Wei, Yu-Xiang Gong, Ri-Ning Tang, Ri-Ning Tang   +7 more
doaj   +2 more sources

Detection and localization of calcium oxalate in kidney using synchrotron deep ultraviolet fluorescence microscopy

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, David Buob, Frédéric Jamme, Chantal Jouanneau, Slavka Kascakova, Jean-Philippe Haymann, Emmanuel Letavernier, Louise Galmiche, Pierre Ronco, Michel Daudon, Dominique Bazin, Matthieu Réfrégiers   +11 more
doaj   +1 more source

Natural History of Clinical, Laboratory, and Echocardiographic Parameters of a Primary Hyperoxaluria Cohort on Long Term Hemodialysis

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, David J. Sas, David J. Sas, Felicity T. Enders, Tina M. Gunderson, Ramila A. Mehta, Julie B. Olson, Barbara M. Seide, Carly J. Banks, Bastian Dehmel, Patricia A. Pellikka, John C. Lieske, John C. Lieske, Dawn S. Milliner, Dawn S. Milliner   +14 more
doaj   +1 more source