Hypokalemia Induced Partial Nephrogenic Diabetes Insipidus: A Case Report [PDF]
Journal of Nepal Medical AssociationDiabetes 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 +4 more
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Use of acetazolamide in lithium-induced nephrogenic diabetes insipidus: a case report [PDF]
Endocrinology, Diabetes & Metabolism Case Reports, 2018 Lithium-induced nephrogenic diabetes insipidus (Li-NDI) is a rare and difficult-to-treat condition. A study in mice and two recent papers describe the use of acetazolamide in Li-NDI in 7 patients (a case report and a 6 patient series).
Ricardo A Macau +4 more
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A Case of Nephrogenic Diabetes Insipidus with a Rare X-linked Recessive Mutation in an Infant with Developmental and Growth Retardation Tracked by the Korean National Health Screening Program [PDF]
Childhood Kidney Diseases, 2020 Nephrogenic diabetes insipidus (DI) is a rare disease in which the patient cannot concentrate urine despite appropriate or high secretion of antidiuretic hormone.
Min-Ji Kim +7 more
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Acute lymphoblastic leukemia with nephrogenic diabetes insipidus as the first symptom: a case report [PDF]
Journal of Medical Case ReportsBackground 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
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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
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Hyperactivation of Nrf2 in early tubular development induces nephrogenic diabetes insipidus
Nature Communications, 2017 Nrf2 regulates oxidative and electrophilic stress responses by modulating the expression of enzymes involved in detoxification pathways. Here Suzukiet al.
Takafumi Suzuki +9 more
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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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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 +10 more
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A case of ifosfamide-induced acute kidney injury, Fanconi syndrome, and nephrogenic diabetes insipidus. [PDF]
CEN Case Rep, 2023 Hoang S +4 more
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Nephrogenic Diabetes Insipidus Affecting Three Males in Two Generations—Case Report and Review of the Literature [PDF]
ChildrenBackground: 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 +6 more
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