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Clinical Case Reports, 2021 Patients with nephrogenic diabetes insipidus should establish a support network system by contacting the government to ensure that water can be preferentially obtained in the event of a disaster and create and carry a medical alert card.
Hiroshi Tamura +5 more
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Endocrine Connections, 2017 Diabetes insipidus is a rare disorder characterized by an impairment in water balance because of the inability to concentrate urine. While central diabetes insipidus is caused by mutations in the AVP, the reason for genetically determined nephrogenic ...
Beril Erdem +5 more
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A Case of Nephrogenic Diabetes Insipidus with a Rare X-linked Recessive Mutation in an Infant with Developmental and Growth Retardation Tracked by the Korean National Health Screening Program [PDF]
Childhood Kidney Diseases, 2020 Nephrogenic diabetes insipidus (DI) is a rare disease in which the patient cannot concentrate urine despite appropriate or high secretion of antidiuretic hormone.
Min-Ji Kim +7 more
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Nephrogenic diabetes insipidus
Current Opinion in Pediatrics, 2017 Purpose of review In nephrogenic diabetes insipidus (NDI), the kidney is unable to concentrate urine despite elevated concentrations of the antidiuretic hormone arginine-vasopressin. In congenital NDI, polyuria and polydipsia are present from birth and should be immediately recognized to avoid severe episodes of
Bockenhauer, D, Bichet, DG
openaire +3 more sources
Indian Journal of Endocrinology and Metabolism, 2011 Fanconi′s syndrome is a complex of multiple tubular dysfunctions of proximal tubular cells occurring alone or in association with a variety of inherited (primary) or acquired (secondary) disorders.
Soumya Patra +5 more
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Diabetes Insipidus: Types, Diagnosis and Management [PDF]
BIO Web of ConferencesDiabetes insipidus (DI) is an acquired or hereditary water imbalance disorder characterized by polydipsia and polyuria. It is a condition that involves the excretion of dilute urine in large volumes.
Jasmeen +5 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
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Saudi Journal of Kidney Diseases and Transplantation, 2018 Systemic lupus erythematosus (SLE) presenting as diabetes insipidus (DI) is a rare association; there is a case report of neurogenic DI in patients of SLE; however, SLE and nephrogenic DI has not been reported in literature.
Ashaq Hussain Parrey +3 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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Therapeutic Advances in Psychopharmacology, 2019 Background: Hypernatraemia is a serious condition that can potentially become life threatening. It is known that lithium is associated with polyuria and nephrogenic diabetes insipidus, risk factors for hypernatraemia.
Michael Ott +2 more
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