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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
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Partial central diabetes insipidus during lithium use: A case report and literature review
PCN ReportsBackground 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 +9 more
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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 +3 more
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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
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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 +3 more
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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 +5 more
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Diabetes insipidus in mice with a mutation in aquaporin-2. [PDF]
PLoS Genetics, 2005 Congenital nephrogenic diabetes insipidus (NDI) is a disease characterized by failure of the kidney to concentrate urine in response to vasopressin. Human kindreds with nephrogenic diabetes insipidus have been found to harbor mutations in the vasopressin
David J Lloyd +3 more
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Idiopathic partial central diabetes insipidus
Einstein (São Paulo), 2023 Diabetes insipidus is a rare disorder characterized by the inability to concentrate urine, which results in hypotonic urine and increased urinary volume.
Larissa Fabre, Viviane Calice da Silva
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Journal of Medical Case Reports, 2020 Background Disorders of water and sodium balance can occur after brain injury. Prolonged polyuria resulting from central diabetes insipidus and cerebral salt wasting complicated by gradient washout and a type of secondary nephrogenic diabetes insipidus ...
Nathan Chang +4 more
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A case of primary aldosteronism combined with acquired nephrogenic diabetes insipidus
Kidney Research and Clinical Practice, 2014 Aldosterone-producing adrenal adenoma can induce various clinical manifestations as a result of chronic exposure to aldosterone. We report a rare case of a 37-year-old man who complained of general weakness and polyuria. He was diagnosed with aldosterone-
Kitae Kim +4 more
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