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Nephrogenic Diabetes Insipidus [PDF]

Pediatric Clinics of North America, 2019
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   +5 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   +2 more sources

Type 1 Bartter syndrome presenting as primary diabetes insipidus: a rare Case Report with 8-year follow-up [PDF]

Frontiers in Genetics
Type 1 Bartter syndrome (BS), a rare autosomal recessive salt-losing tubulopathy, classically presents with hyponatremia, hypochloremia, hypokalemic alkalosis, and hyperreninemic hyperaldosteronism. We report a male patient with the atypical presentation
Huijuan Lu, Shaojun Liu, Jia Sun, Lijun Mou   +3 more
doaj   +2 more sources

Partial central diabetes insipidus during lithium use: A case report and literature review [PDF]

PCN Reports
Background Nephrogenic diabetes insipidus (NDI) is a well‐known adverse effect of lithium, which occurs in approximately 20%–40% of long‐term lithium users.
Mizue Ichinose, Yuri Kobayashi, Yuhei Suzuki, Yoichiro Hirata, Masayuki Goto, Sho Horikoshi, Keiko Kanno‐Nozaki, Kenya Watanabe, Satoshi Takeuchi, Itaru Miura   +9 more
doaj   +2 more sources

Central and nephrogenic diabetes insipidus: updates on diagnosis and management

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   +3 more sources

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   +1 more source

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

Hereditary tubulopathies accompanying polyuia

Regulatory Mechanisms in Biosystems, 2021
Tubulopathies are a group of heterogeneous diseases that are manifested in the malfunction of the renal tubules. This review addresses tubulopathies associated with polyuria syndrome, namely renal glucosuria syndrome, nephrogenic diabetes insipidus and ...
M. O. Ryznychuk, V. P. Pishak, N. V. Bacyuk-Ponych, O. V. Pishak   +3 more
doaj   +1 more source

Nephrogenic Diabetes Insipidus

Apollo Medicine, 2007
A. Sindhwani, D. Singhal, N. Jerath
doaj   +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

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   +1 more source