[Delayed diagnosis of primary hyperoxaluria in a young patient with advanced chronic renal failure]

Nefrologia. 2011;31(2):227-9. doi: 10.3265/Nefrologia.pre2010.Nov.10725.
[Article in Spanish]
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Africa, Northern / ethnology
  • Arthritis, Infectious / complications
  • Bone Marrow Examination
  • Catheter-Related Infections / complications
  • Combined Modality Therapy
  • Decompression, Surgical
  • Delayed Diagnosis
  • Discitis / complications
  • Discitis / surgery
  • Fatal Outcome
  • Humans
  • Hyperoxaluria / complications
  • Hyperoxaluria / diagnosis
  • Hyperoxaluria / genetics
  • Hyperoxaluria, Primary / diagnosis*
  • Hyperoxaluria, Primary / genetics
  • Hyperoxaluria, Primary / pathology
  • Hyperthyroidism / complications
  • Incidental Findings
  • Kidney Failure, Chronic / etiology*
  • Kidney Failure, Chronic / therapy
  • Kidney Failure, Chronic / urine
  • Laminectomy
  • Male
  • Nephrocalcinosis / etiology*
  • Renal Dialysis
  • Thrombophilia / complications
  • Transaminases / deficiency*
  • Transaminases / genetics
  • Vitamin B 6 / therapeutic use
  • Young Adult

Substances

  • Vitamin B 6
  • Transaminases
  • Alanine-glyoxylate transaminase

Supplementary concepts

  • Primary hyperoxaluria type 1