Acta Scientific Medical Sciences (ASMS)(ISSN: 2582-0931)

Case Report Volume 6 Issue 7

A Rare Genetic Disease “Oncogenic Phosphorus Diabetes” Diagnosed in a Nephrological Environment: A Case Report

Leila Belkacemi*

Nephrology, Dialysis and Transplantation Department, CHU Nefissa-Hamoud, Algeria

*Corresponding Author: Leila Belkacemi, Nephrology, Dialysis and Transplantation Department, CHU Nefissa-Hamoud, Algeria.

Received: February 01, 2022; Published: June 01, 2022

Abstract

Phosphorus diabetes is defined by a massive tubular leakage of phosphorus leading to osteomalacia. The etiologies of this syndrome are acquired tubular leaks, hypophosphatemic rickets and oncogenic phosphorus diabetes, the latter having a benign tumor as its pathophysiology [1]; in about 90% of cases; secreting a phosphatonin most often FGF 23 which has the effect of a tubular leakage of phosphorus as well as an inhibition of the synthesis of calcitriol [2].

Keywords: Phosphorus diabetes; osteomalacia;

References

  1. Véronique Breuil. “Diabètes phosphatésPhosphate diabetes”. Revue du Rhumatisme Monographies4 (2012): 253-257.
  2. M Laroche., et al. “Normal FGF23 Levels in Adult Idiopathic Phosphate Diabetes”. Calcified Tissue International2 (2009): 112-117.

Citation

Citation: Leila Belkacemi. “A Rare Genetic Disease “Oncogenic Phosphorus Diabetes” Diagnosed in a Nephrological Environment: A Case Report”.Acta Scientific Medical Sciences 6.7 (2022): 15-16.

Copyright

Copyright: © 2022 Leila Belkacemi. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.




Metrics

Acceptance rate30%
Acceptance to publication20-30 days
Impact Factor1.403

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