Nefropatías congénitas y hereditarias (I)tubulopatías

  1. Gili, B. Quiroga
  2. del Valle, K.M. Pérez
  3. Sevillano, B. Hernández
  4. de la Fuente, G. de Arriba
Zeitschrift:
Medicine: Programa de Formación Médica Continuada Acreditado

ISSN: 0304-5412

Datum der Publikation: 2019

Titel der Ausgabe: Enfermedades nefrourinarias (V)Enfermedades renales tubulointersticiales.Nefropatías hereditarias y congénitas

Serie: 12

Nummer: 83

Seiten: 4878-4884

Art: Artikel

DOI: 10.1016/J.MED.2019.06.022 DIALNET GOOGLE SCHOLAR

Andere Publikationen in: Medicine: Programa de Formación Médica Continuada Acreditado

Zusammenfassung

Tubulopathies comprise a set of inherited or acquired renal disorders presenting ionic abnormalities. According with renal tubule segment involved, tubulopathies are classified in: impairment of proximal tubule (glucosuria, aminoaciduria, phosphaturia, hypouricemia, proximal tubular acidosis type II or Fanconi syndrome which encompasses most of them in a complex way); impairment of Henle's loop and distal tubule (Bartter syndrome, Gitelman syndrome and magnesium depletion); impairment of collecting tubule (Liddle syndrome, tubular acidosis I and IV, and nephrogenic diabetes insipidus). Overall, prognosis is favorable in the most of cases. Treatment requires fluid and electrolyte replacement.

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Fuente de los datos: Dialnet