Results 21 to 30 of about 9,902 (178)

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

An unusual complication of snake bite

open access: yesThe Egyptian Journal of Internal Medicine, 2014
Anterior pituitary hypofunction is a well-known complication following snake bite. However, central diabetes insipidus as a complication of snake bite is only rarely reported in the literature. We are reporting a case of central diabetes insipidus, which
Mary Grace, K C Shanoj
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

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

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

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

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

Central diabetes insipidus secondary to COVID-19 infection: a case report

open access: yesBMC Endocrine Disorders, 2022
Background Novel coronavirus disease 2019 (COVID-19) mainly affects the lungs, but can involve several other organs. The diagnosis of acute and chronic sequelae is one of the challenges of COVID-19.
Ali Yavari   +3 more
doaj   +1 more source

Pengelolaan Central Diabetes Insipidus Pasca Cedera Kepala Berat

open access: yesJurnal Neuroanestesi Indonesia, 2019
Cedera otak traumatika adalah salah satu penyebab kematian dan kesakitan tersering pada kelompok masyarakat muda. Hasil akhir dari cedera kepala berat dapat menyebabkan gangguan kognitif, perilaku, psikologi dan sosial. Salah satu konsekuensi dari cedera
Bona Akhmad Fithrah   +2 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

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