Results 1 to 10 of about 3,546 (164)

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

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

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

Nephrogenic Diabetes Insipidus

Apollo Medicine, 2007
Congenital nephrogenic diabetes insipidus is a rare disorder of resistance to Anti Diuretic Hormone (ADH), characterized by polyuria, polydipsia, low urine osmolality and high serum osmolality. Diagnosis is established by measuring serum and urine osmolality, water deprivation test and vasopressin challenge test. This report describes a 4½-year-old boy
A. Sindhwani, D. Singhal, N. Jerath
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

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 [PDF]

Pediatric Clinics of North America, 2019
Body fluid homeostasis is essential for normal life. In the maintenance of water balance, the most important factor and regulated process is the excretory function of the kidneys. The kidneys are capable to compensate not only the daily fluctuations of water intake but also the consequences of fluid loss (respiration, perspiration, sweating, hemorrhage)
András, Balla, László, Hunyady
openaire   +4 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