Nephrogenic Diabetes Insipidus [PDF]
Nephrogenic diabetes insipidus (NDI) results from the inability of the late distal tubules and collecting ducts to respond to vasopressin. The lack of ability to concentrate urine results in polyuria and polydipsia. Primary and acquired forms of NDI exist in children. Congenital NDI is a result of mutation in AVPR2 or AQP2 genes.
Catherine, Kavanagh, Natalie S, Uy
exaly +7 more sources
Lithium-induced nephrogenic diabetes insipidus following improved medication compliance: a case report [PDF]
Background Nephrogenic diabetes insipidus is a rare, often underrecognized complication of long-term lithium therapy. Lithium-induced nephrogenic diabetes insipidus results from chronic renal exposure, leading to significant polyuria, dehydration, and ...
Eugene Annor +3 more
doaj +3 more sources
Central and nephrogenic diabetes insipidus: updates on diagnosis and management [PDF]
Diabetes insipidus (DI) is a rare endocrine disease involving antidiuretic hormone (ADH), encompassing both central and nephrogenic causes. Inability to respond to or produce ADH leads to inability of the kidneys to reabsorb water, resulting in hypotonic
Thanh D Hoang
exaly +4 more sources
Desmopressin responding female nephrogenic diabetes insipidus: a case report [PDF]
Nephrogenic diabetes insipidus, decreased ability to concentrate urine, with production of large amounts of urine, is caused by the refractory response of renal tubules to the action of antidiuretic hormone.
Juyeon Lee +3 more
doaj +3 more sources
Infant Nephrogenic Diabetes Insipidus: Challenges Leading to Delayed Management. [PDF]
Background Nephrogenic diabetes insipidus (NDI) is a rare, potentially life‐threatening renal tubular disorder characterized by a decreased ability to concentrate urine due to antidiuretic hormone (ADH) resistance, leading to significant free water loss.
Stankovic M S +10 more
europepmc +2 more sources
Early onset of nephrogenic diabetes insipidus due to fabry disease in a child with GLA N215S mutation: Case report and literature review [PDF]
Background: Fabry disease (FD) is a rare X-linked lysosomal storage disorder. Renal involvement in FD is characterized by proteinuria and progressive renal decline.
Zhihong Lu +5 more
doaj +2 more sources
Reversible Nephrogenic Diabetes Insipidus Induced by Lithium: A Case Report. [PDF]
Lithium is an effective mood stabilizer but may cause nephrogenic diabetes insipidus (NDI) by impairing the renal collecting duct response to arginine vasopressin (AVP). We report a 52‐year‐old woman on long‐term lithium therapy who presented with diarrhea, fatigue, polyuria, and confusion.
Uygun İlikhan S +4 more
europepmc +2 more sources
Hypokalemia Induced Partial Nephrogenic Diabetes Insipidus: A Case Report [PDF]
Diabetes insipidus is a condition characterised by a large volume of diluted urine production and increased thirst. In this case report, a 49-year-old gentleman presented with 3 months of polyuria and polydipsia. He had a repeated history of hypokalemia.
Anil Nepali +4 more
doaj +2 more sources
Acute lymphoblastic leukemia with nephrogenic diabetes insipidus as the first symptom: a case report [PDF]
Background Acute lymphoblastic leukemia is the most common pediatric malignancy, characterized by fever, anemia, hemorrhage, and symptoms brought on by blasts infiltrating organs. Case presentation This is a case report of a 9-year-old Asian patient with
Ning Qu, Hongtao Zhu
doaj +2 more sources
Nephrogenic Diabetes Insipidus Affecting Three Males in Two Generations—Case Report and Review of the Literature [PDF]
Background: Nephrogenic diabetes insipidus (NDI) is defined as the inability of the kidney to concentrate urine owing to the insensitivity of the distal nephron to the antidiuretic hormone, arginine vasopressin.
Ramona Stroescu +6 more
doaj +2 more sources

