Results 21 to 30 of about 1,031,173 (193)
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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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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A Pedigree Study of Hereditary Diabetes Insipidus Caused by X Chromosome AVPR2 Gene Mutation [PDF]
International Medical Case Reports JournalLei Li,* Yong Fan,* Guoli Du, Jing Xu, Sheng Jiang State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia; Department of Endocrinology, The First Affiliated Hospital of Xinjiang Medical ...
Li L, Fan Y, Du G, Xu J, Jiang S
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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
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
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Degradation of vasopressin precursor and pathogenic mutants in diabetes insipidus [PDF]
, 2007 The nonapeptide hormone, arginine vasopressin, plays a decisive role in the regulation of fluid balance by reducing free water clearance through reabsorption of water in the renal collecting ducts.
Friberg, Michael
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Fibrillar aggregations of pathogenic pro-vasopressin mutants [PDF]
, 2009 Diabetes insipidus is a disregulation of water homeostasis characterized by large fluid turnover in the kidney. Water homeostasis is regulated by the hormone vasopressin by increasing reapsorption of water in the renal collecting duct. Autosomal dominant
Birk, Julia
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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
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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
openaire +3 more sources
Nephrogenic Diabetes Insipidus Secondary to Obstructive Uropathy – An Unusual Presentation- A Case Report [PDF]
, 2016 Diabetes insipidus is a clinical condition, characterized by polyuria and polydipsia, that results from either insufficient production or end organ resistance to antidiuretic hormone (ADH).
Rahman, MD Azizur +2 more
core +1 more source