LIMITED TREATMENT OPTIONS FOR PRIMARY HYPEROXALURIA WITH RENAL INSUFFICIENCY-Reference-Cited by-同舟云学术

LIMITED TREATMENT OPTIONS FOR PRIMARY HYPEROXALURIA WITH RENAL INSUFFICIENCY

Published:2022-07-15 Issue: Volume: Page:114-115
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Container-title:GLOBAL JOURNAL FOR RESEARCH ANALYSIS
language:en
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Author:

Pate Parth¹,Patel Harsh¹,Javed Syed²

Affiliation:

1. Resident, Department of General Medicine, Geetanjali Medical College And Hospital, Udaipur

2. Associate Professor, Department of General Medicine, Geetanjali Medical College And Hospital, Udaipur.

Abstract

Primary hyperoxaluria (PH) is a rare autosomal recessive metabolic disorder in which the serum levels of oxalate increase because of overproduction.The renal tubule is the primary target of the oxalate deposit, which damages the kidney and leads to cause ESRD. Here, we present a 54-year-old man with a terminal kidney disease; which is dependent on hemodialysis and is likely due to type 2 or 3 PH. Renal insufciency is uncommon to be found in PH patients. With exceedingly high levels of serum oxalate (70 ฀mol/L), this patient had few treatment options available for his rare condition.This report details a unique introduction to a rare condition where renal biopsy was instrumental to reach the diagnosis.

Publisher

World Wide Journals

Reference6 articles.

1. Bouzidi, H., Majdoub, A., Daudon, M., & Najjar, M. F. (2016). Hyperoxalurie primitive : une revue de la littérature. Néphrologie & Thérapeutique, 12(6), 431–436. https://doi.org/10.1016/j.nephro.2016.03.005

2. Primary hyperoxaluria and hyperoxaluria research grants. (2020). Corporate Philanthropy Report, 35(9), 14–15. https://doi.org/10.1002/cprt.30705

3. Kasidas, G., & Rose, G. (1986). Measurement of plasma oxalate in healthy subjects and in patients with chronic renal failure using immobilised oxalate oxidase. Clinica Chimica Acta, 154(1), 49–58. https://doi.org/10.1016/0009-8981(86)90087-2

4. Cai, R., Lin, M., Chen, Z., Lai, Y., Huang, X., Zhao, G., Guo, X., Xiong, Z., Chen, J., Chen, H., Jiang, Q., Liu, S., Yang, Y., Liang, W., Zou, M., Liu, T., Chen, W., Liu, H., & Peng, J. (2019). Primary hyperoxaluria diagnosed after kidney transplantation failure: lesson from 3 case reports and literature review. BMC Nephrology, 20(1). https://doi.org/10.1186/s12882-019-1402-2

5. Giafi, C. F., & Rumsby, G. (1998). Kinetic Analysis and Tissue Distribution of Human D-Glycerate Dehydrogenase/Glyoxylate Reductase and its Relevance to the Diagnosis of Primary Hyperoxaluria Type 2. Annals of Clinical Biochemistry: International Journal of Laboratory Medicine, 35(1), 104–109. https://doi.org/10.1177/000456329803500114