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nephrogenic diabetes insipidus


'nephrogenic diabetes insipidus' can also refer to...

nephrogenic diabetes insipidus

nephrogenic diabetes insipidus

nephrogenic diabetes insipidus

MP090CONGENITAL NEPHROGENIC DIABETES INSIPIDUS IN PREGNANCY

Nephrogenic diabetes insipidus associated with foscarnet—a case report

Hereditary nephrogenic diabetes insipidus: a major conundrum during labour and delivery

Lithium‐induced nephrogenic diabetes insipidus in older people

Nephrogenic diabetes insipidus, thiazide treatment and renal cell carcinoma

Bladder function impairment in aquaporin-2 defective nephrogenic diabetes insipidus

Nephrogenic diabetes insipidus: update of genetic and clinical aspects

Nephrogenic diabetes insipidus, thiazide treatment and renal cell carcinoma

Methotrexate‐induced nephrogenic diabetes insipidus: first case report

Lack of MRI neurohypophyseal bright signal in a child with congenital nephrogenic diabetes insipidus

Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus—update and epidemiology

Low-dose liquorice ingestion resulting in severe hypokalaemic paraparesis, rhabdomyolysis and nephrogenic diabetes insipidus

A de novo novel missense mutation in AVPR2 with severe nephrogenic diabetes insipidus

Mouse models for congenital nephrogenic diabetes insipidus: what can we learn from them?*

Ifosfamide-induced renal Fanconi syndrome with associated nephrogenic diabetes insipidus in an adult patient.

Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus

 

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Quick Reference

(NDI) a condition characterized by polyuria and polydipsia and due to failure of the renal tubules to respond, or to respond fully, to vasopressin. One form of congenital NDI is caused by an X-linked (see sex-linked) dominant mutation of the gene encoding the vasopressin V2 receptor. A rarer form of congenital NDI is an autosomal recessive condition associated with genetic mutations in the gene encoding AQP-2 water channels (see aquaporin). Acquired NDI is much commoner than the congenital form and usually less severe. It is present in most patients with advancing chronic renal failure, is a feature of certain electrolyte disorders (hypokalaemia, hypercalcaemia), and can complicate chronic lithium treatment.

Subjects: Medicine and Health — Chemistry.


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