Dent's Disease

Kidney stones are becoming increasingly common, affecting up to 10% of adults. A small percentage are of monogenic origin, such as Dent's disease (DD). DD is a syndrome that causes low-molecular-weight proteinuria, hypercalciuria, nephrolithiasis, and nephrocalcinosis. It is X-linked, and most...

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Detalles Bibliográficos
Autores: Diéguez, Lucía|||0000-0002-5948-5984, Pilco-Teran, Melissa, Butori, Sofía, Kanashiro, Andrés|||0000-0002-5064-1442, Balañà, Josep|||0000-0001-8248-822X, Emiliani, Esteban|||0000-0003-4488-0022, Somani, Bhaskar K.|||0000-0002-6248-6478, Angerri Feu, Oriol|||0000-0003-3363-6585
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:306944
Acceso en línea:https://ddd.uab.cat/record/306944
https://dx.doi.org/urn:doi:10.3390/jpm14060623
Access Level:acceso abierto
Palabra clave:Dent's disease
Kidney stones
Lithiasis
Monogenic
Descripción
Sumario:Kidney stones are becoming increasingly common, affecting up to 10% of adults. A small percentage are of monogenic origin, such as Dent's disease (DD). DD is a syndrome that causes low-molecular-weight proteinuria, hypercalciuria, nephrolithiasis, and nephrocalcinosis. It is X-linked, and most patients have mutations in the CLCN5 gene. We performed a review of the literature and evaluated the case series (n = 6) of a single center in Spain, reviewing the natural evolution of kidney stones, clinical implications, laboratory analyses, radiological development, and treatment. All patients had a genetically confirmed diagnosis, with the CLCN5 mutation being the most frequent (66%). All patients had proteinuria and albuminuria, while only two and three presented hypercalciuria and phosphate abnormalities, respectively. Only one patient did not develop lithiasis, with most (60%) requiring extracorporeal shock wave lithotripsy or surgery during follow-up. Most of the patients are under nephrological follow-up, and two have either received a renal transplant or are awaiting one. The management of these patients is similar to that with lithiasis of non-monogenic origin, with the difference that early genetic diagnosis can help avoid unnecessary treatments, genetic counseling can be provided, and some monogenic kidney stones may benefit from targeted treatments.