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Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21.

A ParipovićA MaverN StajićJ PutnikS OstojićB AlimpićN IlićA Sarajlija
Published in: Balkan journal of medical genetics : BJMG (2024)
related COXPD21, especially in regard to neurological and developmental aspects of the disease. However, we point out the generalized tubulopathy and early occurrence of CKD in our patient as atypical renal involvement in COXPD21. Additionally, this is the first report of hypothyroidism and hypoparathyroidism in a COXPD21 patient.
Keyphrases
  • chronic kidney disease
  • case report
  • end stage renal disease
  • risk assessment
  • drug induced