hrp0092p1-97 | Pituitary, Neuroendocrinology and Puberty | ESPE2019
Patti Giuseppa
, Scianguetta Saverio
, Balsamo Antonio
, Cappa Marco
, Corbetta Sabrina
, Gaudino Rossella
, Iughetti Lorenzo
, Salerno Maria Carolina
, Napoli Flavia
, Peri Alessandro
, Maghnie Mohamad
, Perrotta Silverio
, Di Iorgi Natascia
Background: Autosomal dominant neurohypophyseal diabetes insipidus (adNDI) is characterized by arginine vasopressin (AVP) deficiency resulting from mutations in the AVP-NPII genePatients and Methods: We analyzed AVP-NPII gene in 13 kindreds with familial NDIAim: To describe the clinical and molecular features of Italian kindreds with adNDIResults</str...