HEREDITARY HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA (CASE REPORT)
https://doi.org/10.24884/1561-6274-2018-22-2-88-96
Abstract
Hereditary hypophosphatemic rickets with hypercalciuria is a very rare autosomal recessive disease, pathogenic base of which is phosphorus reabsorption disorder in proximal nephron with following development of hypophsphatemia, hypercalciuria calcitriol level increase, decrease of parathyroid hormone, osteopenia and bony deformity. This disease refers to hypophosphatemic rickets, due to mutations in the SLC34A3 gene that encodes the sodium-phosphate cotransporter NaPi-IIc, which is responsible for phosphorus reabsorption in the proximal nephron. In this article, we present a clinical observation for a child with atypical manifestations of hereditary hypophosphatemic rickets with hypercalciuria. The clinical examination showed non constant hypophosphatemia, normal values of maximum tubular phosphate transport, absence of calcitriol serum concentrations increase, rachitic changes and bone mineral disorders during a long period of observation. It didn’t allow clinically to identify one of the variants of hypophosphatemic rickets in a child. The diagnosis was confirmed by the results of complete exome sequencing which revealed previously undescribed compound heterozygous mutation c.1382G> A (p.Trp461Ter) in exon 13 and p.1094-3C> T in intron 10 of the SLC34A3 gene. A correct diagnosis allowed us to reconsider the approaches of the treatment: in hereditary rickets recommended only phosphorus supplementation and prescription of vitamin D due to its increased endogenous production.
About the Authors
S. V. PapizhRussian Federation
Svetlana V. Papizh, MD, PhD. Research Clinical Institute for Pediatrics n.a. acad. Y.E. Veltishev, Division of Inherited & Acquired Kidney Diseases
125412 Moscow, Taldomskaya St., 2
Z. R. Bashirova
Russian Federation
Zilya
Zilya Bashirova,MD, Research Clinical Institute for Pediatrics n.a. acad. Y.E. Veltishev, Division of Inherited & Acquired Kidney Diseases
125412 Moscow, Taldomskaya St., 2
,MD, Research Clinical Institute for Pediatrics n.a. acad. Y.E. Veltishev, Division of Inherited & Acquired Kidney Diseases
125412 Moscow, Taldomskaya St., 2
References
1. Tieder M, Modai D, Samuel R et al. Hereditary hypophosphatemic rickets with hypercalciuria. N Engl J Med 1985; 312: 611–617 doi:10.1056/NEJM198503073121003
2. Tieder M, Modai D, Shaked U. et al. «Idiopathic» hypercalciuria and hereditary hypophosphatemic rickets. Two phenotypical expressions of a common genetic defect. N Engl J Med 1987; 316: 125–129 doi:10.1056/NEJM198701153160302
3. Dasgupta D, Wee MJ, Reyes M et al. Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis. Am Soc Nephrol 2014; 25(10): 2366–2375 doi: 10.1681/ASN.2013101085
4. Papizh S, Prikhodina L, Vladimirova T et al. Clinical and genetic heterogeneity of early-onset nephrocalcinosis in children. Ped Nephrol 2017; 32: 1758 doi: 10.1007/s00467-017-3753-x
5. Bergwitz С, Roslin NM, Tieder M et al. SLC34A3 Mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaP-IIc in maintaining phosphate homeostasis. Am J Hum Genet 2006; 78(2): 179–192 doi: 10.1086/499409
6. Negri AL. Hereditary hypophosphatemias: New genes in the bone-kidney axis. Nephrology 2007; 12: 317–320 doi: 10.1111/j.1440-1797.2007.00824.x
7. Phulwani P, Bergwitz C, Jaureguiberry G. et al. Hereditary hypophosphatemic rickets with hypercalciuria and nephrolithiasisidentification of a novel SLC34A3/NaPi-IIc mutation. Am J Med Genet 2011; 155A: 626–633 doi: 10.1002/ajmg.a.33832
8. Tencza AL, Ichikawa S, Dang A et al. Hypophosphatemic rickets with hypercalciuria due to mutation in SLC34A3/Type IIc sodium-phosphate cotransporter: Presentatión as hypercalciuria and nephrolithiasis. J Clin Endocrinol Metab 2009; 94: 4433–4438 doi: 10.1210/jc.2009-1535
9. Yu Y, Sanderson SR, Reyes M et al. Novel NaPi-IIc mutations causing HHRH and idiopathic hypercalciuria in several unrelated families: long-term follow-up in one kindred. Bone 2012; 50(5): 1100–1106 doi:10.1016/j.bone.2012.02.015
10. Habbig S, Beck BB, Hoppe B. Nephrocalcinosis and urolithiasis in children. Kidney Int 2011; 80(12): 1278–1291 doi: 10.1038/ki.2011.336
11. Miyamoto K, Segawa H, Ito M, Kuwahata M. Physiological regulation of renal sodium-dependent phosphate cotransporters. Jpn J Physiol 2004; 54: 93–102 doi: 10.2170/jjphysiol.54.93
12. Payne RB. Renal tubular reabsorption of phosphate (TmP/GFR): indications and interpretation. Ann Clin Biochem 1998; 35: 201–206 doi: 10.1177/000456329803500203 13. Pettifor JM, Thandrayen K. Hypophosphatemic Rickets: Unraveling the Role of FGF23. Calcif Tissue Int 2012; 91: 297–306 doi: 10.1007/s00223-012-9651-0
13. Areses-Trapote R, López-García JA, Ubetagoyena-Arrieta M. et al. Hereditary hypophosphatemic rickets with hypercalciuria: a case report. Nefrologia 2012; 32(4): 529–534 doi: 10.3265/Nefrologia.pre2012.Apr.11321.
14. Segawa H, Kaneko I, Takahashi A et al. Growth-related renal type II Na/Pi cotransporter. J Biol Chem 2002; 277: 19665– 9672 doi: 10.1074/jbc.M200943200
15. Mejia-Gaviria N, Gil-Peña H, Coto E et al. Genetic and clinical peculiarities in a new family with hereditary hypophosphatemic rickets with hypercalciuria: a case report. Orphanet J Rare Dis 2010; 5: 1 doi: 10.1186/1750-1172
16. Kremke B, Bergwitz C, Ahrens W et al. Hypophosphatemic rickets with hypercalciuria due to mutation in SLC34A3/NaPi-IIc can be masked by vitamin D deficiency and can be associated with renal calcifications. Exp Clin Endocrinol Diabetes 2009; 117: 49–56 doi: 10.1055/s-2008-1076716
17. Carpenter TO, Imel EA, Holm IA et al. A clinician’s guide to X-linked hypophosphatemia. J Bone Miner Res 2011; 26:1381–1388. doi: 10.1002/jbmr.340
18. Li Y, Caballero D, Ponsetto J et al. Response of Npt2a knockout mice to dietary calcium and phosphorus. PLoS One 2017; 12(4): e0176232 doi: 10.1371/journal.pone.0176232
Review
For citations:
Papizh S.V., Bashirova Z.R. HEREDITARY HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA (CASE REPORT). Nephrology (Saint-Petersburg). 2018;22(2):88-96. (In Russ.) https://doi.org/10.24884/1561-6274-2018-22-2-88-96