Results 71 to 80 of about 9,902 (178)

Antidiuretic hormone deficiency secondary to inactive hydrocephalus: a case report

Journal 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, Nikita Kharal, Srijana Sapkota, Prakash Pokhrel, Arun Kumar Sharma, Aseem Bhattarai, Mithileshwer Raut, Raju Kumar Dubey, Eans Tara Tuladhar, Vijay Kumar Sharma, Apeksha Niraula   +10 more
doaj   +1 more source

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

Archives 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, Rodolfo Russo, Francesca Spanò, Diego Ferone, Manuela Albertelli, Angelo Schenone, Miriam Contatore, Andrea Guastalla, Annamaria De Bellis, Giacomo Garibotto, Francesco Puppo   +10 more
doaj   +1 more source

Central Diabetes insipidus in a Nigerian child : A case report

Nigerian 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  

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

Case 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, Resmy Palliyil Gopi, Bina Shah   +2 more
doaj   +1 more source

Idiopathic central diabetes Insipidus.

Indian 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, Venu, Balachandran, Sooraj, Menon   +2 more
openaire   +1 more source

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

Pediatria 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, Małgorzata Barbara Stańczyk, Elżbieta Szczepanik, Katarzyna Monika Krawiranda, Anita Janus, Kacper Piotr Kościelny, Marcin Tkaczyk   +6 more
doaj   +1 more source

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

Journal 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, Reza Manouchehri Ardakani   +1 more
doaj   +1 more source

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

Arquivos 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, MAYER JUNIOR JOSÉ RONALDO, ROCHA MÔNICA ROSAS, KRUGER RODRIGO, TITTON JOÃO ALCEU   +4 more
doaj  

Central diabetes insipidus [PDF]

, 2020
openaire   +1 more source

Central diabetes insipidus

Central 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