Tolvaptan treatment for severe neonatal autosomal-dominant polycystic kidney disease

BACKGROUND: Severe neonatal autosomal-dominant polycystic kidney disease (ADPKD) is rare and easily confused with recessive PKD. Managing such infants is difficult and often unsuccessful. CASE DIAGNOSIS/TREATMENT: A female infant with massive renal enlargement, respiratory compromise and hyponatraem...

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Detalles Bibliográficos
Autores principales: Gilbert, Rodney D., Evans, Hazel, Olalekan, Kazeem, Nagra, Arvind, Haq, Mushfequr R., Griffiths, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368203/
https://www.ncbi.nlm.nih.gov/pubmed/28194574
http://dx.doi.org/10.1007/s00467-017-3584-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368203/
https://www.ncbi.nlm.nih.gov/pubmed/28194574
http://dx.doi.org/10.1007/s00467-017-3584-9

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