Results 41 to 50 of about 4,644 (193)
Tenofovir indcued reversible nephrogenic diabetes insipidus without fanconi syndrome in a patient with hepatitis b [PDF]
, 2018 Background In patients with Hepatitis B Virus, there are approximately 10 cases of Tenofovir related Fanconi Syndrome but no report of nephrogenic diabetes insipidus.
Hein, Y +6 more
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Copeptin-based diagnosis of diabetes insipidus
Swiss Medical Weekly, 2020 Polyuria-polydipsia syndrome consists of the three main entities: central or nephrogenic diabetes insipidus and primary polydipsia. Reliable distinction between these diagnoses is essential as treatment differs substantially, with the wrong treatment ...
Julie Refardt, Mirjam Christ-Crain
doaj +1 more source
Nephrogenic diabetes insipidus in children [PDF]
, 2014 Congenital nephrogenic diabetes insipidus (NDI) is a disorder associated with mutations in either the AVP2R or AQP2 gene, causing the inability of patients to concentrate their pro-urine, which leads to a high risk of dehydration.
Nine V. A. M. Knoers +3 more
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Nephrogenic Diabetes Insipidus - A Rare Report of Two Affected Sibling [PDF]
, 2018 Nephrogenic Diabetes Insipidus (NDI) is a type of Diabetes Insipidus (DI) where distal nephrons are unresponsive to antidiuretic hormone resulting in polyuria and polydipsia. NDI can be congenital or acquired.
Rumana Riaaz +3 more
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Platelet vasopressin receptors in patients with congenital nephrogenic diabetes insipidus [PDF]
, 1991 Platelet vasopressin receptors in patients with congenital nephrogenic diabetes insipidus. Arginine-vasopressin(AVP), interacts with at least two types of receptors: V1 receptors which mediate the aggregating effects of AVP on human blood platelets and ...
Bichet, Daniel G. +2 more
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Acquired Bartter Syndrome in Primary Sjögren Syndrome
Saudi Journal of Kidney Diseases and Transplantation, 2020 Renal tubular involvement in Sjögren's syndrome (SS) often described with renal tubular acidosis, nephrogenic diabetes insipidus, or rarely with Fanconi syndrome.
Aya Fraj +6 more
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Clinical Genetics, Volume 110, Issue 2, Page 203-209, August 2026.We identified a novel pathogenic AVP variant in two Danish families with autosomal dominant inheritance of symptoms of AVP deficiency. In addition, we compiled a catalogue of additionally 109 AVP variants that cause AVP deficiency and demonstrated the advantage of combining expert‐assisted curation, literature search, and online repositories to ensure ...
Jennifa Joseph +5 more
wiley +1 more source
Vasopressin V2 receptor-related pathologies: congenital nephrogenic diabetes insipidus and nephrogenic syndrome of inappropiate antidiuresis [PDF]
, 2014 International audienceCongenital nephrogenic diabetes insipidus is a rare hereditary disease with mainly an X-linked inheritance (90% of the cases) but there are also autosomal recessive and dominant forms.
Morin, Denis
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Hypokalemia Induced Partial Nephrogenic Diabetes Insipidus: A Case Report
Journal of Nepal Medical AssociationDiabetes insipidus is a condition characterised by a large volume of diluted urine production and increased thirst. In this case report, a 49-year-old gentleman presented with 3 months of polyuria and polydipsia. He had a repeated history of hypokalemia.
Anil Nepali +4 more
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Clinical Insights Into Hypercalcemia of Malignancy in Childhood
Pediatric Blood &Cancer, Volume 73, Issue 7, July 2026.ABSTRACT Hypercalcemia of malignancy (HCM) is a rare but life‐threatening metabolic emergency in children that occurs in less than 1% of pediatric cancer cases, with a reported incidence ranging from 0.4% to 1.0% across different studies. While it is observed in 10%–20% of adult malignancies, pediatric HCM remains relatively uncommon.
Hüseyin Anıl Korkmaz
wiley +1 more source