Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case report

BACKGROUND: Congenital nephrogenic diabetes insipidus (NDI) is a rare condition characterized by severe polyuria, due to the inability of the kidneys to concentrate urine in response to arginine vasopressin (AVP). In the majority of the cases, the disease shows an X‐linked inherited pattern, althoug...

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Detalles Bibliográficos
Autores principales: Peces, Ramón, Mena, Rocío, Peces, Carlos, Santos‐Simarro, Fernando, Fernández, Luis, Afonso, Sara, Lapunzina, Pablo, Selgas, Rafael, Nevado, Julián
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465731/
https://www.ncbi.nlm.nih.gov/pubmed/30784238
http://dx.doi.org/10.1002/mgg3.568

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465731/
https://www.ncbi.nlm.nih.gov/pubmed/30784238
http://dx.doi.org/10.1002/mgg3.568

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