Results 11 to 20 of about 3,615 (161)
Infant Nephrogenic Diabetes Insipidus: Challenges Leading to Delayed Management. [PDF]
Case Rep MedBackground 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
Reversible Nephrogenic Diabetes Insipidus Induced by Lithium: A Case Report. [PDF]
Case Rep NephrolLithium 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
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
doaj +2 more sources
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
doaj +1 more source
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
doaj +1 more source
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
doaj +1 more source
Clinical Case Reports, 2021 Nephrogenic diabetes insipidus (NDI) is rarely considered against more common differentials such as diabetes mellitus in patients presenting with polydipsia and polyuria.
Esmail Sangey +2 more
doaj +1 more source
Clinical Case Reports, 2021 Patients with nephrogenic diabetes insipidus should establish a support network system by contacting the government to ensure that water can be preferentially obtained in the event of a disaster and create and carry a medical alert card.
Hiroshi Tamura +5 more
doaj +1 more source
Endocrine Connections, 2017 Diabetes insipidus is a rare disorder characterized by an impairment in water balance because of the inability to concentrate urine. While central diabetes insipidus is caused by mutations in the AVP, the reason for genetically determined nephrogenic ...
Beril Erdem +5 more
doaj +1 more source
Nephrogenic diabetes insipidus
Current Opinion in Pediatrics, 2017 Purpose of review In nephrogenic diabetes insipidus (NDI), the kidney is unable to concentrate urine despite elevated concentrations of the antidiuretic hormone arginine-vasopressin. In congenital NDI, polyuria and polydipsia are present from birth and should be immediately recognized to avoid severe episodes of
Bockenhauer, D, Bichet, DG
openaire +3 more sources