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Kidney diabetes insipidus
Last reviewed: 23.04.2024
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Causes of the renal insipid diabetes
Renal diabetes insipidus develops due to the lack of sensitivity of epithelial cells of the distal tubules to arginine-vasopressin (antidiuretic hormone), which is mainly due to mutation of the V1 receptor gene of arginine-vasopressin (X-linked form). In addition, the cause is a mutation of the gene encoding the water channel associated with the V2 receptor, aquaporin-2 (an autosomal recessive form of inheritance).
Acquired renal insipid diabetes develops in many diseases.
Symptoms of the renal insipid diabetes
Primary renal diabetes insipidus is diagnosed in the first week of life.
Symptoms are typical: polyuria, multiple vomiting, convulsions; often expressed dehydration and hyponatremia.
In older children, polyuria, nocturia, polydipsia are found.
Forms
Congenital renal diabetes insipidus
- Mutations of V1-receptor genes of antidiuretic hormone.
- Mutation of the aquaporin-2 gene.
Acquired renal diabetes insipidus
- Medicines:
- lithium preparations;
- amphotericin B.
- Nicotine.
- Alcohol.
- Chronic renal failure (especially in the outcome of tubulointerstitial nephritis and obstructive uropathy).
- Sickle-cell anemia.
- Amyloidosis.
- Disease and Sjogren's syndrome.
- Sarcoidosis.
- Hypercalcemia.
- Cystinosis.
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Treatment of the renal insipid diabetes
Treatment consists in the appointment of hydrochlorothiazide, potassium preparations, abundant drinking.
Also justified is the limited sodium intake. Secondary renal diabetes insipidus can be completely eliminated by treatment of the underlying disease.
Drugs