# Ultrasound diagnosis of nephrocalcinosis in an infant with recurrent vomiting

**Authors:** Marta Cecilia Carrasco Hidalgo-Barquero, Luis Ortiz-Peces, Luis Ortiz-González

PMC · DOI: 10.1016/j.aprim.2026.103458 · 2026-02-13

## Full-text entities

- **Genes:** CLDN19 (claudin 19) [NCBI Gene 149461] {aka HOMG5}, CLDN16 (claudin 16) [NCBI Gene 10686] {aka HOMG3, PCLN1}
- **Diseases:** acidosis tubular renal distal (MESH:D000141), Bartter (MESH:D001477), vomiting (MESH:D014839), nephrocalcinosis (MESH:D009397), renal cronica (MESH:D006030), hipervitaminosis D (MESH:D014808), tubulopatia hereditaria (MESH:C535730)
- **Chemicals:** Se (MESH:D012643), ambos (-)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12925261/full.md

---
Source: https://tomesphere.com/paper/PMC12925261