Results 71 to 80 of about 10,133 (174)

Issues of differential diagnosis and management of central diabetes insipidus / differential diagnosis and management of central diabetes insipidus

open access: yesМедицинский совет, 2018
Diabetes insipidus (DI) is a syndrome characterized by the excretion of abnormally large volumes of diluted urine. It can be caused by two fundamentally different defects that must be distinguished for safe and effective management.
G. R. Vagapova
doaj   +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

Feeding difficulties in infancy as an early symptom of different forms of diabetes insipidus – a series of cases

open access: yesPediatria Polska
Feeding disorders of infancy are common in paediatric practice. Among rare causes of this disturbance is diabetes insipidus (DI), which is a clinical syndrome characterized by polyuria, polydypsia and dehydration with hypernatraemia.
Katarzyna Anna Banasiak   +6 more
doaj   +1 more source

Diabetes insipidus as a presentation of lung adenocarcinoma: a case report

open access: yesJournal of Medical Case Reports
Background Paraneoplastic syndromes are rare complications associated with malignancies, and central diabetes insipidus represents one of their uncommon manifestations.
Maryam Alsadat Tabatabaei   +1 more
doaj   +1 more source

Genotype-based severity scoring system in Wolfram Syndrome: correlation with onset of cardinal symptoms and WFS1 gene variant types

open access: yesFrontiers in Genetics
BackgroundWolfram syndrome is a rare genetic disorder characterized by antibody‐negative early‐onset atypical diabetes mellitus, optic nerve atrophy, sensorineural hearing loss, central diabetes insipidus (arginine vasopressin deficiency), and ...
Liam Oiknine   +11 more
doaj   +1 more source

Generalized status epilepticus associated with massive pulmonary aspiration and transient central diabetes insipidus: case report

open access: yesArquivos de Neuro-Psiquiatria, 2000
Status epilepticus causes significant morbidity and mortality. A case of generalized status epilepticus followed by massive pulmonary aspiration, acute respiratory failure and transient central diabetes insipidus is presented.
CARVALHO MAURICIO   +4 more
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

Central diabetes insipidus

open access: yesCentral diabetes insipidus
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.
openaire  

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