Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family

• Váldodahkkit: Myo-Jing Kim (Dahkki), Young-Eun Kim (Dahkki), Chang-Seok Ki (Dahkki), Jae-Ho Yoo (Dahkki)
• Materiálatiipa: Girji
• Almmustuhtton: Korean Society of Pediatric Endocrinology, 2014-12-01T00:00:00Z.
• Fáttát: article
• Liŋkkat: Connect to this object online.

Autosomal dominant neurohypophyseal diabetes insipidus is a rare form of central diabetes insipidus that is caused by mutations in the vasopressin-neurophysin II (AVP-NPII) gene. It is characterized by persistent polydipsia and polyuria induced by deficient or absent secretion of arginine vasopressi...