Results 31 to 40 of about 6,941,594 (151)

Central diabetes insipidus and burn trauma

open access: yesScars, Burns & Healing, 2022
Diabetes insipidus (DI) is characterized by polyuria and polydipsia. In most cases, the condition results from either an inadequate release or resistance to the activity of antidiuretic hormone in the renal collecting tubules. The underlying pathophysiology may be related to destruction the destruction or degeneration of neurons from inflammatory ...
Jonathan Kopel   +5 more
openaire   +3 more sources

Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family [PDF]

open access: yesAnnals of Pediatric Endocrinology & Metabolism, 2014
Autosomal dominant neurohypophyseal diabetes insipidus is a rare form of central diabetes insipidus that is caused by mutations in the vasopressin-neurophysin II (AVP-NPII) gene.
Myo-Jing Kim   +3 more
doaj   +1 more source

Efficacy of Indapamide in Central Diabetes Insipidus [PDF]

open access: yesArchives of Internal Medicine, 1999
Central diabetes insipidus (CDI) results from deficient vasopressin (antidiuretic hormone) secretion and causes polydipsia and polyuria. Desmopressin, a synthetic analog of vasopressin, is the drug of choice in the treatment of CDI, but in mild cases, there are alternative drugs that can be used, including chlorpropamide, carbamazepine, and thiazides ...
T, Tetiker, M, Sert, M, Koçak
openaire   +2 more sources

Central Diabetes insipidus in a Nigerian child : A case report [PDF]

open access: yes, 2014
Background: Central diabetes insipidus (CDI) is rare in children. About 30 - 50% of cases are idiopathic. Early and accurate diagnosis are crucial for safe and effective treatment.
Anochie, IC, Yarhere, I, Okpere, AN
core   +1 more source

Diabetes insípida como forma de apresentação de leucemia mielóide aguda.

open access: yesActa Médica Portuguesa, 2004
Central diabetes insipidus, is a syndrome characterized by the excretion of abnormally elevated volumes of diluted urine, due to the diminution of reabsorption of water in the collecting ducts, induced by the diminution of production of antidiuretic ...
Susana Calretas   +5 more
doaj   +1 more source

Thunderclap headache caused by a pituitary non-functioning tumour presenting as spontaneous pituitary apoplexy [PDF]

open access: yesRomanian Journal of Neurology, 2010
Hemorrhagic or ischemic pituitary apoplexy is a rare neuro-endocrine emergency, potentially leading to coma. Neuro-ophthalmic symptoms or complications are amongst the most prevalent clinical features at onset, especially in previously asymptomatic ...
Carmen E. Georgescu   +5 more
doaj   +1 more source

Gradient washout and secondary nephrogenic diabetes insipidus after brain injury in an infant: a case report

open access: yesJournal 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

Non-urological cause of bilateral hydroureteronephrosis

open access: yesIndian Journal of Urology, 2021
Bilateral hydroureteronephrosis in a patient with central diabetes insipidus is a rare condition. This rare presentation poses unique diagnostic and therapeutic challenges.
Jatin Soni   +3 more
doaj   +1 more source

Pituitary dysfunction with eosinophilic granulomatosis with polyangiitis presenting with diabetes insipidus: a case report and review of the literature

open access: yesFrontiers in Immunology
Central 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   +1 more source

Developmental Glaucoma with Central Diabetes Insipidus: A Case Report and Review of Literature

open access: yesDelhi Journal of Ophthalmology, 2016
Association of developmental glaucoma with diabetes insipidus is a rare condition with only single citation as a part of DIDMOAD syndrome. However it has never been previously reported as an association with isolated diabetes insipidus.
Piyush Kumar R Ramavat   +6 more
doaj   +1 more source

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