Distar Renal Tubular Acidosis (dRTA): Epidemiological, diagnostics, clinical follow-up and therapeutical issues. Nephrologists cohort survey outcome

Distar Renal Tubular Acidosis (dRTA): Epidemiological, diagnostics, clinical follow-up and therapeutical issues. Nephrologists cohort survey outcome

Background and objectives: dRTA is a genetic or acquired rare disease, characterized by an unability to excrete hydrogens (H+) into urine, hypobicarbonatemia, hyperchloremia, and frequently hypercalciuria and hypokalaemia. Genetic forms are usually diagnosed during the first months of life and its t...

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Bibliographic Details
Main Authors: José Vicente Torregrosa Prats, Fernando Santos Rodríguez, Emilio González Parra, Laura Espinosa Román, Juan Manuel Buades Fuster, Enrique Monteagud-Marrahí, Victor Manuel Navas Serrano
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:Nefrología (English Edition)
Subjects:
Acidosis tubular renal distal
Calciuria
Hipobicarbonatemia
Hipokaliemia
Enfermedad renal crónica
Enfermedad ósea
Online Access:http://www.sciencedirect.com/science/article/pii/S201325142100002X

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http://www.sciencedirect.com/science/article/pii/S201325142100002X

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