Ambarsari, Cahyani Gita and Agianda, Habibah Azzahra Putri and Saraswati, Meilania and Kim, Jon Jin (2025) Dent Disease 1 Presented Early with Bartter-Like Syndrome Features and Rickets: A Case Report. Case Reports in Nephrology and Dialysis, 15 (1). 15 - 25. ISSN 22969705
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Abstract
Introduction: Dent disease (DD) is characterized by a triad of low-molecular-weight proteinuria, hypercalciuria, and nephrocalcinosis/nephrolithiasis. However, some cases were confounded by other clinical symptoms and signs, namely, hypokalemia and rickets, which resulted in misleading diagnoses. A diagnosis of DD could be delayed even in high-resource countries due to its variability of phenotypes and rarity, causing a lack of awareness in both medical practitioners and parents. Moreover, in low-resource countries, laboratory test limitations can hinder the diagnosis. Case Presentation: A thirteen-year-old boy presented with an acute episode of severe hypokalemia following vomiting due to COVID medication side effects. He had lower extremities weakness, salt craving, and polydipsia since childhood which were not thought to be unusual by the parents. He had a history of intrauterine polyhydramnios and maternal miscarriages. A physical examination showed hypotension, short stature, and genu valgum. His laboratory workup displayed hypokalemic metabolic alkalosis and increased urine potassium, chloride, transtubular potassium gradient, and calcium/creatinine ratio. He also had hypophosphatemia, hypomagnesemia, and decreased kidney function. Severe osteopenia was prominent on radiologic examination of all extremities. Subsequent laboratory samples sent overseas revealed low-molecular-weight proteinuria and a pathogenic variant in the CLCN5 gene confirming X-linked DD 1. Conclusion: This case report highlights the importance of considering DD in differential diagnoses of children with the pseudo-Bartter syndrome, that is, renal salt and potassium wasting, with or without hypercalciuria and nephrocalcinosis. Additionally, in children with rickets and proteinuria, urinary low-molecularweight protein measurement could assist in screening for the possibility of DD, particularly in low-resource settings. ©2025 The Author(s). Published by S. Karger AG, Basel.
| Item Type: | Article |
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| Additional Information: | Cited by: 1; All Open Access; Gold Open Access; Green Open Access |
| Uncontrolled Keywords: | chloride; creatinine; magnesium; ondansetron; paracetamol; potassium; potassium dihydrogen phosphate; ramipril; vitamin D; adolescent; Article; Bartter syndrome; blood group ABO incompatibility; case report; cesarean section; child; chloride channel gated 5 gene; clinical article; coronavirus disease 2019; creatinine blood level; creatinine clearance; Dent disease; dent disease 1; echography; end stage renal disease; failure to thrive; family history; fatigue; gene; glomerulosclerosis; home quarantine; human; human cell; human tissue; hypochloremia; hypokalemia; hypokalemic metabolic alkalosis; hypomagnesemia; hypophosphatemia; hypotension; jaundice; kidney biopsy; kidney calcification; kidney function; kidney parenchyma; male; metabolic alkalosis; muscle cramp; muscle weakness; nausea and vomiting; nephrolithiasis; nocturia; osteopenia; physical examination; placenta previa; polydipsia; polyhydramnios; polyuria; potassium urine level; proteinuria; radiodiagnosis; rickets; school child; short stature; spontaneous abortion; stillbirth; tibia torsion; twin pregnancy; valgus knee; vitamin supplementation; vomiting; whole genome sequencing |
| Subjects: | R Medicine > RB Biomedical Sciences |
| Divisions: | Faculty of Medicine, Public Health and Nursing > Biomedical Sciences |
| Depositing User: | Yuliawati Dahniar Dahniar |
| Date Deposited: | 06 Aug 2026 04:31 |
| Last Modified: | 06 Aug 2026 04:31 |
| URI: | https://ir.lib.ugm.ac.id/id/eprint/28480 |
