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Here, we describe a Swiss family with an autosomal dominant mutation in the AVP gene region encoding for the carrier protein neurophysin II (P55R). In addition, we discuss the algorithm for diagnosing and treating patients with hereditary CDI based on this Swiss family.<\/jats:p>","DOI":"10.1210\/jcemcr\/luac023","type":"journal-article","created":{"date-parts":[[2022,12,3]],"date-time":"2022-12-03T09:33:05Z","timestamp":1670059985000},"source":"Crossref","is-referenced-by-count":0,"title":["Diagnosis and Treatment of Hereditary Central Diabetes Insipidus in a Swiss Family With a Mutation in the <i>AVP<\/i> Gene"],"prefix":"10.1210","volume":"1","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9958-9705","authenticated-orcid":false,"given":"Lorena","family":"Wyniger","sequence":"first","affiliation":[{"name":"Department of Endocrinology, Diabetology and Metabolism, University Hospital Basel , 4031 Basel , Switzerland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nicole","family":"Beuret","sequence":"additional","affiliation":[{"name":"Biozentrum, University of Basel , 4056 Basel , 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