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Comment
. 2017 Apr;32(4):609-613.
doi: 10.1007/s00467-016-3440-3. Epub 2016 Jul 6.

Rare case of nephrocalcinosis in a 14-year-old girl: Answers

Omar Bjanid  1 , Piotr Adamczyk  2 , Małgorzata Stojewska  2 , Dagmara Roszkowska-Bjanid  1 , Magdalena Paszyna-Grześkowiak  1 , Agnieszka Jędzura  1 , Joanna Oświęcimska  2 , Katarzyna Ziora  2 , Aurelia Morawiec-Knysak  1 , Maria Szczepańska  3
Affiliations
Comment

Rare case of nephrocalcinosis in a 14-year-old girl: Answers

Omar Bjanid et al. Pediatr Nephrol. 2017 Apr.
No abstract available

Keywords: Autoimmune polyendocrine syndrome type 1; Calcium supplementation; Hypercalciuria; Hypoparathyroidism; Nephrocalcinosis.

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Conflict of interest statement

The authors declare that they have no conflicts of interest.

Figures

Fig. 1
Fig. 1
Tubular disorders with hypercalciuric nephrocalcinosis. dRTA Distal renal tubular acidosis, UAG urine anion gap, Sd syndrome, LMW low molecular weight, FHHNC familial hypomagnesemia with hypercalciuria and nephrocalcinosis,TmP/GFR renal tubular maximum reabsorption rate of phosphate to glomerular filtration rate, NaPi sodium/phosphate cotransporter
See this image and copyright information in PMC

Comment on

  • Rare case of nephrocalcinosis in a 14-year-old girl: Questions.
    Bjanid O, Adamczyk P, Stojewska M, Roszkowska-Bjanid D, Paszyna-Grześkowiak M, Jędzura A, Oświęcimska J, Ziora K, Morawiec-Knysak A, Szczepańska M. Bjanid O, et al. Pediatr Nephrol. 2017 Apr;32(4):607-608. doi: 10.1007/s00467-016-3434-1. Epub 2016 Jul 6. Pediatr Nephrol. 2017. PMID: 27384690 Free PMC article.

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