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Endocrinology, Diabetes & Metabolism Case Reports, 2018 The combination of hyperosmolar hyperglycaemic state and central diabetes insipidus is unusual and poses unique diagnostic and therapeutic challenges for clinicians.
Snezana Burmazovic +3 more
doaj +1 more source
Nagoya journal of medical science, 2016 Central diabetes insipidus (CDI), characterized by polyuria and polydipsia, is caused by deficiency of arginine vasopressin (AVP), an antidiuretic hormone which acts on V2 receptors in kidney to promote reabsorption of free water. CDI is classified into three subtypes; idiopathic, secondary and familial.
Arima, Hiroshi +3 more
openaire +2 more sources
Central diabetes insipidus and burn trauma
Scars, 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
Thunderclap headache caused by a pituitary non-functioning tumour presenting as spontaneous pituitary apoplexy [PDF]
Romanian 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
An unusual complication of snake bite
The 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
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family [PDF]
Annals 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
Non-urological cause of bilateral hydroureteronephrosis
Indian 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
Diabetes insípida como forma de apresentação de leucemia mielóide aguda.
Acta 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
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
doaj +1 more source
Developmental Glaucoma with Central Diabetes Insipidus: A Case Report and Review of Literature
Delhi 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