Results 21 to 30 of about 1,896 (180)
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
Central diabetes insipidus secondary to COVID-19 infection: a case report
BMC Endocrine Disorders, 2022 Background Novel coronavirus disease 2019 (COVID-19) mainly affects the lungs, but can involve several other organs. The diagnosis of acute and chronic sequelae is one of the challenges of COVID-19.
Ali Yavari +3 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
Frontiers in ImmunologyCentral diabetes insipidus secondary to hypophysitis in eosinophilic granulomatosis with polyangiitis (EGPA) is very rare, and this article summarizes one case reported from our site as well as two previously reported patients with EGPA, both of whom had
Aifei Zhang +6 more
doaj +1 more source
Pengelolaan Central Diabetes Insipidus Pasca Cedera Kepala Berat
Jurnal Neuroanestesi Indonesia, 2019 Cedera otak traumatika adalah salah satu penyebab kematian dan kesakitan tersering pada kelompok masyarakat muda. Hasil akhir dari cedera kepala berat dapat menyebabkan gangguan kognitif, perilaku, psikologi dan sosial. Salah satu konsekuensi dari cedera
Bona Akhmad Fithrah +2 more
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Sheehan's syndrome with central diabetes insipidus [PDF]
Arquivos Brasileiros de Endocrinologia & Metabologia, 2011 Sheehan's syndrome refers to the occurrence of hypopituitarism after delivery, usually preceded by postpartum hemorrhage. The condition still continues to be a common cause of hypopituitarism in developing countries like India. The disorder usually presents with anterior pituitary failure with preservation of posterior pituitary functions.
Bashir Ahmad, Laway +3 more
openaire +2 more sources
Ожирение и метаболизм, 2018 Diabetes insipidus (DI) is a rare syndrome characterized by an excretion of abnormally large volumes of diluted urine and a corresponding increase in fluid intake.
Ekaterina A. Pigarova
doaj +1 more source