scholarly journals Ifosfamide-induced nephrogenic diabetes insipidus responsive to supraphysiologic doses of intravenous desmopressin

2021 ◽  
Vol 9 (1) ◽  
pp. 87-92
Author(s):  
Mohammad A. Sohail ◽  
Mohamed Hassanein ◽  
Hernan Rincon-Choles
Keyword(s):  
Diabetes Insipidus ◽  
Nephrogenic Diabetes Insipidus

scholarly journals Congenital nephrogenic diabetes insipidus accompanied with central nephrogenic diabetes secondary to pituitary surgery -a case report

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Wei Zhang ◽  
Yimin Shen ◽  
Yuezhong Ren ◽  
Yvbo Xin ◽  
Lijun Wang
Keyword(s):  
Diabetes Insipidus ◽  
Nephrogenic Diabetes Insipidus ◽  
Direct Detection ◽  
Urine Volume ◽  
Pituitary Surgery ◽  
Accurate Method ◽  
Heterozygous Mutation ◽  
Case Presentation ◽  
Congenital Nephrogenic Diabetes Insipidus

Abstract Background Diabetes insipidus (DI) can be a common cause of polydipsia and polyuria. Here, we present a case of congenital nephrogenic diabetes insipidus (CNDI) accompanied with central diabetes insipidus (CDI) secondary to pituitary surgery. Case presentation A 24-year-old Chinese woman came to our hospital with the complaints of polydipsia and polyuria for 6 months. Six months ago, she was detected with pituitary apoplexy, and thereby getting pituitary surgery. However, the water deprivation test demonstrated no significant changes in urine volume and urine gravity in response to fluid depression or AVP administration. In addition, the genetic results confirmed a heterozygous mutation in arginine vasopressin receptor type 2 (AVPR2) genes. Conclusions She was considered with CNDI as well as acquired CDI secondary to pituitary surgery. She was given with hydrochlorothiazide (HCTZ) 25 mg twice a day as well as desmopressin (DDAVP, Minirin) 0.1 mg three times a day. There is no recurrence of polyuria or polydipsia observed for more than 6 months. It can be hard to consider AVPR2 mutation in female carriers, especially in those with subtle clinical presentation. Hence, direct detection of DNA sequencing with AVPR2 is a convenient and accurate method in CNDI diagnosis.

scholarly journals A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothers

2016 ◽  
Vol 175 (5) ◽  
pp. 727-733 ◽  
Author(s):  
Marie Helene Schernthaner-Reiter ◽  
David Adams ◽  
Giampaolo Trivellin ◽  
Mary Scott Ramnitz ◽  
Margarita Raygada ◽  
...  
Keyword(s):  
Diabetes Insipidus ◽  
Splice Site ◽  
Nephrogenic Diabetes Insipidus ◽  
Splice Site Mutation ◽  
Site Mutation

Intravenous Dopamine Associated with Nephrogenic Diabetes Insipidus-Like Syndrome

1999 ◽  
Vol 17 (2) ◽  
pp. 167-169
Author(s):  
Arieh Oppenheim ◽  
Reuven Pizov ◽  
Michal Elhallel-Darnitzki ◽  
Yosef S. Haviv
Keyword(s):  
Diabetes Insipidus ◽  
Nephrogenic Diabetes Insipidus

Misfolded vasopressin V2 receptors caused by extracellular point mutations entail congential nephrogenic diabetes insipidus

2000 ◽  
Vol 164 (1-2) ◽  
pp. 31-39 ◽  
Author(s):  
Rolf Postina ◽  
Elke Ufer ◽  
Roland Pfeiffer ◽  
Nine V.A.M. Knoers ◽  
Falk Fahrenholz
Keyword(s):  
Diabetes Insipidus ◽  
Nephrogenic Diabetes Insipidus ◽  
Point Mutations
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