Results 21 to 30 of about 44,873 (216)

Central diabetes insipidus unmasked by kidney transplantation: a case report and literature review

open access: yesTransplantation Reports, 2020
Background: Diabetes insipidus (DI) is a relatively uncommon abnormality of water homeostasis resulting in the excess production of hypotonic polyuria. Post-transplant polyuria is typically self-limited and resolves without intervention.
Shaheed Merani, MD PhD FRCSC FACS   +3 more
doaj   +1 more source

Transient Diabetes Insipidus in a Preterm Neonate: An Uncommon Cause of Neonatal Shock

open access: yesIndian Pediatrics Case Reports, 2022
Background: Diabetes insipidus (DI) is a disorder of water homeostasis due to insufficient production or inappropriate action of vasopressin. Central DI (CDI) develops due to intracranial causes such as hypoxic–ischemic encephalopathy, meningitis, and ...
Gouda Ankula Prasad Kartikeswar   +3 more
doaj   +1 more source

Management of diabetes insipidus in children

open access: yesIndian Journal of Endocrinology and Metabolism, 2011
Diabetes Insipidus (DI) is a heterogeneous clinical syndrome of disturbance in water balance, characterized by polyuria (urine output > 4 ml/kg/hr), polydypsia (water intake > 2 L/m 2 /d) and failure to thrive.
Garima Mishra, Sudha Rao Chandrashekhar
doaj   +1 more source

Tachycardia-polyuria syndrome after swan-ganz catheterization in liver transplant patient - A case report - [PDF]

open access: yesAnesthesia and Pain Medicine, 2021
Background Tachycardia-polyuria syndrome is characterized by polyuria occurring because of tachycardia with a heart rate of ≥ 120 beats/min lasting ≥ 30 min. We report such a case occurring after swan-ganz catheterization.
Sang-Kwon Heo   +3 more
doaj   +1 more source

Diabetes insipidus: The other diabetes

open access: yesIndian 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.
Sanjay Kalra   +9 more
doaj   +1 more source

Transient Antenatal Bartter’s Syndrome: A Case Report

open access: yesFrontiers in Pediatrics, 2018
Antenatal Bartter’s syndrome is a rare inherited disorder characterized by fetal polyhydramnios and polyuria that is usually detected between 24 and 30 weeks of gestation. However, a rare, severe, but transient form of antenatal Bartter’s syndrome due to
Michelle Meyer   +2 more
doaj   +1 more source

Transient central diabetes insipidus following ischemic stroke

open access: yesIndian Journal of Endocrinology and Metabolism, 2013
Central Diabetes Insipidus (CDI) following ischemic infarction of the brain has been described as a rare presentation. Posterior pituitary ischemia has also been postulated as a possible cause of idiopathic CDI. We encountered a young male with bilateral
Muthukrishnan Jayaraman   +2 more
doaj   +1 more source

Disseminated tuberculosis presenting as hypovolemic shock, hypernatremia with central diabetes insipidus

open access: yesJournal of Pediatric Critical Care, 2020
Disseminated tuberculosis (TB) not uncommon in children in developing countries like India, and the spectrum of the disease varies in the different age groups.
Ramaning Loni   +4 more
doaj   +1 more source

Insipidary syndrome in children and adolescents (part 2)

open access: yesЛечащий Врач, 2021
The review article presents current data on water-electrolyte balance in healthy and pathological state. The diseases and conditions which occur in insipidary syndrome are described.
V. V. Smirnov, L. I. Bikbaeva
doaj  

Decreased nitric oxide production is a novel therapeutic target for salt-induced nocturnal polyuria in aging. [PDF]

open access: yesSci Rep
Nocturnal polyuria is a major cause of nocturia, which affects quality of life. Aging-related decreases in nitric oxide production have been reported to contribute to salt-induced nocturnal polyuria.
Imanaka T   +11 more
europepmc   +2 more sources

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