Idiopathic infantile hypercalcemia in children with chronic kidney disease due to kidney hypodysplasia

Background Idiopathic infantile hypercalcemia (IIH) etiologies include pathogenic variants in CYP24A1 , leading to increased 1,25(OH) 2 D, hypercalciuria and suppressed parathyroid hormone (PTH), and in SLC34A1 and SLC34A3 , leading to the same metabolic profile via increased phosphaturia. IIH has n...

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Veröffentlicht in:Pediatric nephrology (Berlin, West) West), 2023-04, Vol.38 (4), p.1067-1073
Hauptverfasser: Gurevich, Evgenia, Borovitz, Yael, Levi, Shelli, Perlman, Sharon, Landau, Daniel
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Sprache:eng
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Zusammenfassung:Background Idiopathic infantile hypercalcemia (IIH) etiologies include pathogenic variants in CYP24A1 , leading to increased 1,25(OH) 2 D, hypercalciuria and suppressed parathyroid hormone (PTH), and in SLC34A1 and SLC34A3 , leading to the same metabolic profile via increased phosphaturia. IIH has not been previously described in CKD due to kidney hypodysplasia (KHD). Methods Retrospective study of children with bilateral KHD and simultaneously tested PTH and 1,25(OH) 2 D, followed in a tertiary care center between 2015 and 2021. Results Of 295 screened patients, 139 had KHD, of them 16 (11.5%) had IIH (study group), 26 with normal PTH and any 1,25(OH) 2 D were controls. There were no differences between groups’ gender, obstructive uropathy rate and baseline eGFR. Study patients were younger [median (IQR) age: 5.2 (3.2–11.3) vs. 61 (13.9–158.3) months, p  
ISSN:0931-041X
1432-198X
DOI:10.1007/s00467-022-05740-w