Síndrome de Bartter como causa de polihidramnios severo. A propósito de un caso / Bartter syndrome as a cause of severe polyhydramnios. Apropos of a case
Clín. investig. ginecol. obstet. (Ed. impr.)
; 43(1): 43-45, ene.-mar. 2016. tab
Article
in Spanish
| IBECS
| ID: ibc-148455
Responsible library:
ES1.1
Localization: BNCS
RESUMEN
El síndrome de Bartter es una rara enfermedad congénita que afecta a los túbulos renales. Se presenta el caso de una paciente que debutó en la semana 32 con polihidramnios severo de aparición brusca, como única manifestación de esta enfermedad, diagnosticada posnatalmente
ABSTRACT
Bartter syndrome is a rare congenital disease that affects the renal tubules. We describe the case of a patient with onset of severe polyhydramnios at 32 weeks of gestation, as the only clinic manifestation of this disease, which was diagnosed postnatally
Full text:
Available
Collection:
National databases
/
Spain
Database:
IBECS
Main subject:
Bartter Syndrome
/
Polyhydramnios
Type of study:
Diagnostic study
/
Etiology study
Limits:
Adult
/
Female
/
Humans
/
Pregnancy
Language:
Spanish
Journal:
Clín. investig. ginecol. obstet. (Ed. impr.)
Year:
2016
Document type:
Article
Institution/Affiliation country:
Hospital Río Hortega/España
/
Hospital de Medina del Campo/España