Heterozygous mutations of the gene for Kir 1.1 (ROMK) in antenatal Bartter syndrome presenting with transient hyperkalemia, evolving to a benign course.

Bartter-like syndrome encompasses a set of inherited renal tubular disorders associated with hypokalemic metabolic alkalosis, renal salt wasting, hyperreninemic hyperaldosteronism, and normal blood pressure. Antenatal Bartter syndrome, a subtype of Bartter-like syndrome, is characterized by polyhydr...

Descripción completa

Detalles Bibliográficos
Autores principales: Cho, Jong Tae, Guay-Woodford, Lisa Marie
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 2003
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3055000/
https://www.ncbi.nlm.nih.gov/pubmed/12589089

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3055000/
https://www.ncbi.nlm.nih.gov/pubmed/12589089

Ejemplares similares