Results 81 to 90 of about 6,941,594 (151)

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

BMC 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, Yu-Cheng Liang, Meng-Jie Tsai, Horng-Yih Ou   +3 more
doaj   +1 more source

Kidney, Pituitary, Eyes, and Nose Involved in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis: A Case Report and Literature Review

Case Reports in Nephrology and Dialysis
Introduction: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a systemic autoimmune disease characterized by diverse clinical manifestations.
Xiaonan Feng, Yinyin Yan, Na Tian, Lihua Wu   +3 more
doaj   +1 more source

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

Медицинский 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

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

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

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

Arginine vasopressin deficiency (central diabetes insipidus) with partial empty sella: a case report

BMC Endocrine Disorders
Background Arginine vasopressin deficiency (central diabetes insipidus) is defined as a reduction in the release of arginine vasopressin (AVP) resulting in a variable degree of polyuria. Partial empty sella refers to an enlarged sella turcica that is not
Kibret Enyew Belay, Rebil H. Jemal, Ayele H. Kebede, Meron G. Tulu, Alamirew Enyew Belay, Asteway Mulat Haile, Samuel A. Demisse   +6 more
doaj   +1 more source

Etiologic evaluation of central diabetes insipidus in fourty-one patient

, 2000
Amaç: Santral diabetes insipidus tanısı ile takip edilen kırkbir hastanın etiyolojik yönden değerlendirilmesidir. Çalışmanın Yapıldığı Yer: Çalışma, Çukurova Üniversitesi Tıp Fakültesi, Pediatrik Endokrinoloji ve Metabolizma Bilimdalında yapıldı ...
Zehra Can, Önenli Neslihan Mungan, Güler Özer, Bilgin Yüksel, Dinçer Yıldızdaş   +4 more
core   +1 more source

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

Frontiers 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, Abby F. Tang, Evan M. Lee, Nila Palaniappan, Megha Verma, Kasra Vand, Sahiti Somalraju, Sarath Chandra Janga, Sarath Chandra Janga, Sarath Chandra Janga, Fumihiko Urano, Fumihiko Urano   +11 more
doaj   +1 more source