Results 71 to 80 of about 1,896 (180)

Antidiuretic hormone deficiency secondary to inactive hydrocephalus: a case report

open access: yesJournal of Medical Case Reports
Background Diabetes insipidus is a syndrome characterized by polyuria, which is almost always associated with polydipsia. The most frequent cause is central diabetes insipidus, which is the result of an inadequate secretion of the antidiuretic hormone ...
Anuradha Kadel   +10 more
doaj   +1 more source

Sheehan’s syndrome presenting with panhypopituitarism and central diabetes insipidus: a case report

open access: yesBMC Endocrine Disorders
Background 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   +1 more source

Autoimmune central diabetes insipidus in a patient with ureaplasma urealyticum infection and review on new triggers of immune response

open access: yesArchives of Endocrinology and Metabolism, 2015
Diabetes insipidus is a disease in which large volumes of dilute urine (polyuria) are excreted due to vasopressin (AVP) deficiency [central diabetes insipidus (CDI)] or to AVP resistance (nephrogenic diabetes insipidus).
Giuseppe Murdaca   +10 more
doaj   +1 more source

A Case of Transient Central Diabetes Insipidus after Aorto-Coronary Bypass Operation [PDF]

open access: gold, 2012
Chung-Hoon Yu   +12 more
openalex   +1 more source

Use of Chlorothiazide in the Management of Central Diabetes Insipidus in Early Infancy

open access: yesCase Reports in Pediatrics, 2017
Management of central diabetes insipidus in infancy is challenging. The various forms of desmopressin, oral, subcutaneous, and intranasal, have variability in the duration of action.
Manish Raisingani   +2 more
doaj   +1 more source

Diabetes insipidus in neuropsychiatric-systemic lupus erythematosus patient

open access: yesIndonesian Journal of Rheumatology, 2018
Systemic lupus erythematosus (SLE) is an idiopathic autoimmune chronic inflammatory disease that is unique in its diversity of clinical manifestations, variability of disease’s progression, and prognosis.
Y Pangestu   +10 more
doaj   +1 more source

Clinical presentation and outcome of children with central diabetes insipidus associated with a self‐limited or transient pituitary stalk thickening, diagnosed as infundibuloneurohypophysitis [PDF]

open access: hybrid, 2017
Jacqueline Schaefers   +8 more
openalex   +1 more source

Central Diabetes insipidus in a Nigerian child : A case report

open access: yesNigerian Journal of Paediatrics
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.
Okpere AN, Anochie IC , Yarhere I
doaj  

Idiopathic central diabetes Insipidus.

open access: yesIndian journal of medical sciences, 2013
Idiopathic central diabetes insipidus (CDI) is a rare disorder characterized clinically by polyuria and polydipsia, and an abnormal urinary concentration without any identified etiology. We report a case of central diabetes insipidus in a 60-year-old lady in the absence of secondary causes like trauma, infection, and infiltrative disorders of brain.
Mary, Grace   +2 more
openaire   +1 more source

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