An overview of Dent disease
Dent disease is a rare inherited kidney tubulopathy caused by mutations in either the CLCN5 (Dent disease 1) or OCRL1 (Dent disease 2) genes, and which is often underdiagnosed in practice. A diagnosis is clinically suspected in patients with low-molecular-weight proteinuria, hypercalciuria, and one...
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Main Authors: | Eun Mi Yang (Author), Seong Hwan Chang (Author) |
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Format: | Book |
Published: |
Korean Society of Pediatric Nephrology,
2023-12-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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