Results 21 to 30 of about 3,615 (161)
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
doaj +1 more source
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]
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
doaj +1 more source
Unsuspected nephrogenic diabetes insipidus
Long term treatment with lithium can lead to nephrogenic diabetes insipidus by making distal renal tubules resistant to the action of vasopressin.1–3 Polyuria and polydipsia are the likely clinical features, but the condition may not always be clinically apparent; especially when the underlying condition has not been recognised.
A, Waise, R A, Fisken
openaire +3 more sources
Diabetes Insipidus: Types, Diagnosis and Management [PDF]
Diabetes 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
doaj +1 more source
Persistent Nephrogenic Diabetes Insipidus After Discontinuation of Lithium: A Case Report [PDF]
In this article, a case with diabetes insipidus starting with lithium tratment and persisting after discontinuation is presented. The patient complained about being thirsty, polydipsia, and polyuria for 5 months.
Aysun Kalenderoğlu +4 more
doaj
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
doaj +1 more source
Copeptin-based diagnosis of diabetes insipidus
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
Acquired Bartter Syndrome in Primary Sjögren Syndrome
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
doaj +1 more source
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
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
doaj +1 more source

