primary oxalosis
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F1000Research ◽  
2021 ◽  
Vol 10 ◽  
pp. 914
Author(s):  
Ben Mrad Imtinene ◽  
Kamoun Sofien ◽  
Ben Mrad Melek ◽  
Zairi Ihsen ◽  
Oumaya Zeineb ◽  
...  

Primary hyperoxaluria (PH) type 1 is a rare hereditary metabolic disorder resulting in accumulation of calcium oxalate in several organs, including the heart. Cardiac oxalosis in PH is poorly described in the medical literature. We report the case of a 42-year-old woman diagnosed with primary hyperoxaluria type 1 and end-stage renal failure who presented with syncope related to a paroxysmal third-degree atrioventricular block. The patient benefited from the implantation of a dual chamber pacemaker with a good outcome. Conduction blocks in case of primary hyperoxaluria type 1 are exceptional; in fact, less than five reports have previously been published in the medical literature. With this case, we would like to highlight the need for regular and careful monitoring of cardiac status in patients treated for primary oxalosis, especially when renal function is impaired.


2020 ◽  
Vol 55 (4) ◽  
pp. 192-192
Author(s):  
Stefano Fratoni ◽  
Pasquale Niscola

2020 ◽  
Vol 18 (6) ◽  
pp. 744-748
Author(s):  
Omar AlShalabi ◽  
Ebru H. Ayvazoglu Soy ◽  
Aydincan Akdur ◽  
Emre Karakaya ◽  
Gokhan Kahraman ◽  
...  

2015 ◽  
Vol 13 (2) ◽  
pp. 97-99
Author(s):  
Ayse Sinangil ◽  
Vedat Celik ◽  
Soykan Barlas ◽  
Fatih Altunrende ◽  
Emin Baris Akin ◽  
...  

Abstract Hyperoxaluria type I (HPI) is a metabolic disorder secondary to liver alanine glyoxylate aminotransferase deficiency. Renal failure occurs due to the excessive production and precipitation of oxalate in the kidney. Combined liver-renal transplantation is the correct treatment for this condition when end-stage renal failure occurs since in renal transplantation alone the risk of recurrence of the same pathology in the transplanted kidney would be high. We determined the calcification surrounding the double J stent inserted to the transplant ureter in a short time in a 22-year-old patient who underwent sequential liver and renal transplantation with the diagnoses of oxalosis. In the literature we have not found papers on calcification of double J stent following combined or sequential transplantation. Although after the sequential transplantation the calcification, nephrocalcinosis, and renal stones were practically not of great concern, these patients should be followed up more carefully in terms of stent calcification during the early post-transplant period.


Author(s):  
Bernard Puech ◽  
Jean-Jacques De Laey
Keyword(s):  

2013 ◽  
Vol 39 (10) ◽  
pp. 1843-1844
Author(s):  
Nazi Benhenda ◽  
Anne Bernard-Brunet ◽  
Martine Ferrandière ◽  
Ephrem Salamé ◽  
Dominique Babuty

2012 ◽  
Vol 7 (3) ◽  
pp. 458-465 ◽  
Author(s):  
Jérôme Harambat ◽  
Karlijn J. van Stralen ◽  
Laura Espinosa ◽  
Jaap W. Groothoff ◽  
Sally-Anne Hulton ◽  
...  

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