Diagnosis and Treatment of Hereditary Central Diabetes Insipidus in a Swiss Family With a Mutation in the AVP Gene

Hereditary central diabetes insipidus (CDI) is a genetic disorder characterized by polydipsia and polyuria. Most known mutations are located in the arginine-vasopressin (AVP) gene. Here, we describe a Swiss family with an autosomal dominant mutation in the AVP gene region encoding for the carrier pr...

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Detalles Bibliográficos
Autores principales: Wyniger, Lorena, Beuret, Nicole, Rutishauser, Jonas, Seelig, Eleonora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578377/
https://www.ncbi.nlm.nih.gov/pubmed/37908243
http://dx.doi.org/10.1210/jcemcr/luac023

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578377/
https://www.ncbi.nlm.nih.gov/pubmed/37908243
http://dx.doi.org/10.1210/jcemcr/luac023

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