Abstract Diabetes Insipidus (DI) is a rare disease which can be or central and peripheral (nephrogenic) forms, primary or secondary, or combined. Primary disease is of hereditary origin and caries some kind of inheritance like X-linked or recessive forms which are already described. In these article an interesting case of Diabetes Insipidus is described in a female patient of Armenian nationality with family history of diabetes mellitus. The diagnosis was made due to specific blood and urine tests specific for DI.
A concomitant condition such as autoimmune thyroiditis has been also diagnosed. Improvement of patient’s condition due to desmopressin therapy was an additional probe of diagnosis. Recommendations: to be very careful in each case of polyuria and polydipsia in any age period of life. Introduction: Diabetes insipidus (diabetes insipidus; syndrome of diabetes insipidus (DI);…
