Dent disease (Q98836): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A doença de Dent é uma doença tubular renal genética rara, caracterizada por manifestações de disfunção do túbulo proximal com proteinúria de baixo peso molecular (BPM) e hipercalciúria, nefrolitíase, nefrocalcinose e insuficiência renal progressiva. | |||
| description / en | description / en | ||
Dent disease is a rare genetic renal tubular disease characterised by manifestations of proximal tubule dysfunction with low-molecular-weight (LMW) proteinuria and hypercalciuria, nephrolithiasis, nephrocalcinosis, and progressive renal failure. | |||
Revision as of 15:27, 16 August 2026
Dent disease is a rare genetic renal tubular disease characterised by manifestations of proximal tubule dysfunction with low-molecular-weight (LMW) proteinuria and hypercalciuria, nephrolithiasis, nephrocalcinosis, and progressive renal failure.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1762998355 |
||
| English | Dent disease |
Dent disease is a rare genetic renal tubular disease characterised by manifestations of proximal tubule dysfunction with low-molecular-weight (LMW) proteinuria and hypercalciuria, nephrolithiasis, nephrocalcinosis, and progressive renal failure. |
