Congenital and acquired diseases related to stone formation

Curr Opin Urol. 2018 Sep;28(5):414-419. doi: 10.1097/MOU.0000000000000522.

Abstract

Purpose of review: To summarize the latest findings of congenital and acquired diseases related to stone formation and help understanding the multitude of cofactors related to urolithiasis.

Recent findings: Urolithiasis is related to a broad spectrum of congenital and acquired diseases and its management varies according to the stone type, underlying disease or recurrence rate, but it also changes according to recent findings and developments. As prevalence of urolithiasis is constantly increasing, identification of high-risk stone formers and early treatment is essential. Therefore, genetic evaluation like whole exome sequencing becomes a pertinent part of further diagnostics.

Summary: Stone formation is a very heterogeneous pathomechanism. This prompt us to look at every patient individually particularly in high-risk patients, including stone and 24-h-urine analysis and additional diagnostic work-up based on stone type or underlying disease.

Publication types

  • Review

MeSH terms

  • Acidosis, Renal Tubular / epidemiology
  • Adenine Phosphoribosyltransferase / deficiency
  • Cystic Fibrosis / epidemiology
  • Cystinuria / epidemiology
  • Dent Disease / epidemiology
  • Drug-Related Side Effects and Adverse Reactions
  • Humans
  • Hyperoxaluria, Primary / epidemiology
  • Hyperparathyroidism / epidemiology
  • Immobilization / statistics & numerical data
  • Inflammatory Bowel Diseases / epidemiology
  • Lesch-Nyhan Syndrome / epidemiology
  • Metabolic Syndrome / epidemiology
  • Metabolism, Inborn Errors / epidemiology
  • Nephrocalcinosis / epidemiology
  • Polycystic Kidney Diseases / epidemiology
  • Risk Factors
  • Sarcoidosis / epidemiology
  • Spinal Cord Injuries / epidemiology
  • Urinary Bladder, Neurogenic / epidemiology
  • Urinary Tract Infections / epidemiology
  • Urolithiasis / epidemiology*
  • Xanthine Dehydrogenase / deficiency

Substances

  • Xanthine Dehydrogenase
  • Adenine Phosphoribosyltransferase

Supplementary concepts

  • Adenine phosphoribosyltransferase deficiency