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Nature Reviews Disease Primers, 2019 Diabetes insipidus is a rare but treatable condition that typically presents with extreme thirst (polydipsia) together with the passing of large amounts of dilute urine (polyuria).
Mirjam Christ-Crain +6 more
semanticscholar +9 more sources
Pediatrics in Review, 2020 A disorder characterized by excretion of large amounts of urine, accompanied by excessive thirst. Causes include deficiency of antidiuretic hormone or failure of the kidneys to respond to antidiuretic hormone. It may also be drug-related.
Alyson Weiner, Patricia Vuguin
semanticscholar +3 more sources
La Presse Médicale, 2021 Diabetes insipidus (DI) is a disorder characterized by a high hypotonic urinary output of more than 50ml per kg body weight per 24 hours, with associated polydipsia of more than 3 liters a day [1,2]. Central DI results from inadequate secretion and usually deficient synthesis of Arginine vasopressin (AVP) in the hypothalamus or pituitary gland. Besides
Mirjam Christ-Crain, Odile Gaisl
semanticscholar +3 more sources
Pituitary dysfunction with eosinophilic granulomatosis with polyangiitis presenting with diabetes insipidus: a case report and review of the literature [PDF]
Frontiers in ImmunologyCentral diabetes insipidus secondary to hypophysitis in eosinophilic granulomatosis with polyangiitis (EGPA) is very rare, and this article summarizes one case reported from our site as well as two previously reported patients with EGPA, both of whom had
Aifei Zhang +6 more
doaj +2 more sources
Frontiers in Endocrinology, 2019 Adipsic Diabetes Insipidus is a rare hypothalamic disorder characterized by a loss of thirst in response to hypernatraemia accompanied by diabetes insipidus.
Rinkoo Dalan +9 more
doaj +2 more sources
Diabetes insipidus: The other diabetes
Indian Journal of Endocrinology and Metabolism, 2016 Diabetes insipidus (DI) is a hereditary or acquired condition which disrupts normal life of persons with the condition; disruption is due to increased thirst and passing of large volumes of urine, even at night.
S. Kalra +9 more
semanticscholar +5 more sources
Lithium-induced nephrogenic diabetes insipidus following improved medication compliance: a case report [PDF]
Journal of Medical Case ReportsBackground 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 +3 more
doaj +2 more sources
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 dehydration ...
D. Bockenhauer, D. Bichet
semanticscholar +5 more sources
Journal of Clinical Endocrinology and Metabolism, 2022 Recent data show that patients with a diagnosis of diabetes insipidus (DI) are coming to harm. Here we give the rationale for a name change to arginine vasopressin deficiency and resistance for central and nephrogenic DI, respectively.
Hiroshi Arima +10 more
semanticscholar +2 more sources
Sheehan’s syndrome presenting with panhypopituitarism and central diabetes insipidus: a case report [PDF]
BMC Endocrine DisordersBackground Sheehan’s syndrome is a rare condition, which is classically characterized by anterior pituitary hypofunction following postpartum shock or hemorrhage.
Chin-Fang Chen +3 more
doaj +2 more sources