Dent’s disease: case series from a single center
DD is a disease that shows different phenotypes even among individuals with mutations in the same gene. Therefore, it should be considered in all patients with hypercalciuria, proteinuria, nephrolithiasis or nephrocalcinosis with/without proximal tubular dysfunction especially in the early childhood period. Classical treatments for hypercalciuria should be utilized, and a patient-based treatment plan should be drawn especially for proteinuria.
Authors
- Emre Leventoğlu (ORCID: https://orcid.org/0000-0002-0504-7911)
- Bahar Büyükkaragöz (ORCID: https://orcid.org/0000-0002-6342-1975)
- Oğuz Söylemezoğlu (ORCID: https://orcid.org/0000-0002-9861-884X)
- Sevcan Azime Bakkaloglu (ORCID: https://orcid.org/0000-0001-6530-9672)
- Hilal Yaşar (ORCID: https://orcid.org/0009-0002-8897-9446)
- Kibriya Fidan (ORCID: https://orcid.org/0000-0001-8210-5313)
Institutions
- Gazi University (TR)
Publication Details
- Journal
- The Turkish Journal of Pediatrics
- Published
- 2024-11-11
- DOI
- https://doi.org/10.24953/turkjpediatr.2024.4556
- Citations
- 1
- Primary Topic
- Neonatal Health and Biochemistry
- Type
- article
- Field-Weighted Citation Impact
- 1.11