Clinical Heterogeneity and Phenotypic Expansion of NaPi-IIa-Associated Disease

J Clin Endocrinol Metab. 2017 Dec 1;102(12):4604-4614. doi: 10.1210/jc.2017-01592.


Context: NaPi-IIa, encoded by SLC34A1, is a key phosphate transporter in the mammalian proximal tubule and plays a cardinal role in renal phosphate handling. NaPi-IIa impairment has been linked to various overlapping clinical syndromes, including hypophosphatemic nephrolithiasis with osteoporosis, renal Fanconi syndrome with chronic kidney disease, and, most recently, idiopathic infantile hypercalcemia and nephrocalcinosis.

Objectives: We studied the molecular basis of idiopathic infantile hypercalcemia with partial proximal tubulopathy in two apparently unrelated patients of Israeli and Turkish descent.

Design: Genetic analysis in two affected children and their close relatives was performed using whole-exome sequencing, followed by in vitro localization and trafficking analysis of mutant NaPi-IIa.

Results: Mutation and haplotype analyses in both patients revealed a previously described homozygous loss-of-function inserted duplication (p.I154_V160dup) in NaPi-IIa, which is inherited identical-by-descent from a common ancestor. The shared mutation was originally reported by our team in two adult siblings with renal Fanconi syndrome, hypophosphatemic bone disease, and progressive renal failure who are family members of one of the infants reported herein. In vitro localization assays and biochemical analysis of p.I154_V160dup and of additional NaPi-IIa mutants harboring a trafficking defect indicate aberrant retention at the endoplasmic reticulum in an immature and underglycosylated state, leading to premature proteasomal degradation.

Conclusions: Our findings expand the phenotypic spectrum of NaPi-IIa disruption, reinforce its link with proximal tubular impairment, enable longitudinal study of the natural history of the disease, and shed light on cellular pathways associated with loss of function and impaired trafficking of NaPi-IIa mutants.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Endoplasmic Reticulum / pathology
  • Exome / genetics
  • Fanconi Anemia / pathology
  • Fanconi Syndrome / genetics*
  • Gene Duplication
  • Haplotypes
  • Humans
  • Hypercalcemia / genetics*
  • Infant
  • Kidney Diseases / complications
  • Male
  • Mutation / genetics
  • Pedigree
  • Phenotype
  • Proteasome Endopeptidase Complex
  • Renal Insufficiency, Chronic / pathology
  • Sodium-Phosphate Cotransporter Proteins, Type IIa / genetics*


  • SLC34A1 protein, human
  • Sodium-Phosphate Cotransporter Proteins, Type IIa
  • Proteasome Endopeptidase Complex