Results 1 to 10 of about 8,398 (199)

Desmopressin responding female nephrogenic diabetes insipidus: a case report [PDF]

Childhood Kidney Diseases, 2022
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, Hae Il Cheong, Jung Won Lee, Ki Soo Pai   +3 more
doaj   +4 more sources

Lithium-induced nephrogenic diabetes insipidus following improved medication compliance: a case report [PDF]

Journal of Medical Case Reports
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, Ishita Bhattacharya, Mary Bass, Emily M. Horvath   +3 more
doaj   +4 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]

Heliyon, 2023
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, Yan Wang, Langping Gao, Li Lin, Lidan Hu, Jianhua Mao   +5 more
doaj   +2 more sources

A novel mutation affecting the arginine-137 residue of AVPR2 in dizygous twins leads to nephrogenic diabetes insipidus and attenuated urine exosome aquaporin-2 [PDF]

, 2016
Mutations in the vasopressin V2 receptor gene AVPR2 may cause X-linked nephrogenic diabetes insipidus by defective apical insertion of aquaporin-2 in the renal collecting duct principal cell.
Dieperink, Hans, Fagerberg, Christina, Hinrichs, Gitte R, Houlberg Hansen, Louise, Jensen, Boye L, Nielsen, Maria R, Rittig, Søren   +6 more
core   +3 more sources

Hypokalemia Induced Partial Nephrogenic Diabetes Insipidus: A Case Report [PDF]

Journal of Nepal Medical Association
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, Prakriti Adhikari, Amit Shah, Shailes Paudel, Prakriti Bhandari   +4 more
doaj   +2 more sources

Acute lymphoblastic leukemia with nephrogenic diabetes insipidus as the first symptom: a case report [PDF]

Journal of Medical Case Reports
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

Central and nephrogenic diabetes insipidus: updates on diagnosis and management [PDF]

Frontiers in Endocrinology
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
Kathryn Flynn, Jennifer Hatfield, Kevin Brown, Nicole Vietor, Thanh Hoang   +4 more
doaj   +2 more sources

AKAPs-PKA disruptors increase AQP2 activity independently of vasopressin in a model of nephrogenic diabetes insipidus

Nature Communications, 2018
Patients suffering from congenital nephrogenic diabetes insipidus (NDI) fail to concentrate urine due to mutations in vasopressin type 2 receptor (V2R). Here Ando et al.
Fumiaki Ando, Shuichi Mori, Naofumi Yui, Tetsuji Morimoto, Naohiro Nomura, Eisei Sohara, Tatemitsu Rai, Sei Sasaki, Yoshiaki Kondo, Hiroyuki Kagechika, Shinichi Uchida   +10 more
doaj   +2 more sources

Nephrogenic diabetes insipidus with idiopathic Fanconi′s syndrome in a child who presented as vitamin D resistant rickets

Indian Journal of Endocrinology and Metabolism, 2011
Fanconi′s syndrome is a complex of multiple tubular dysfunctions of proximal tubular cells occurring alone or in association with a variety of inherited (primary) or acquired (secondary) disorders.
Soumya Patra, Gulnaz Nadri, Harish Chowdhary, Harish K Pemde, Varinder Singh, Jagdish Chandra   +5 more
doaj   +2 more sources

Nephrogenic Diabetes Insipidus Affecting Three Males in Two Generations—Case Report and Review of the Literature [PDF]

Children
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, Adela Chiriţă-Emandi, Maria Puiu, Flavia Chisavu, Ruxandra Steflea, Gabriela Doroş, Mihai Gafencu   +6 more
doaj   +2 more sources