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Diagnosis is often based on urine tests, blood tests and the fluid deprivation test. [1] Despite the name, diabetes insipidus is unrelated to diabetes mellitus and the conditions have a distinct mechanism, though both can result in the production of large amounts of urine. [1] Treatment involves drinking sufficient fluids to prevent dehydration ...
Type 1 is the most common form of diabetes in dogs and affects approximately 0.34% of dogs. [8] Type 2 diabetes can develop in dogs, although it is not as prevalent as type 1. [9] Because of this, there is no possibility the permanently damaged pancreatic beta cells could re-activate to engender a remission as may be possible with some feline ...
Fluid deprivation test. A fluid or water deprivation test is a medical test [ 1] which can be used to determine whether the patient has diabetes insipidus as opposed to other causes of polydipsia (a condition of excessive thirst that causes an excessive intake of water). The patient is required, for a prolonged period, to forgo intake of water ...
Rare. Chronic multifocal Langerhans cell histiocytosis, previously known as Hand–Schüller–Christian disease, [ 3][ 4] is a type of Langerhans cell histiocytosis (LCH), which can affect multiple organs. [ 1][ 5][ 6] The condition is traditionally associated with a combination of three features; bulging eyes, breakdown of bone (lytic bone ...
Desmopressin. Desmopressin, sold under the trade name DDAVP among others, is a medication used to treat diabetes insipidus, bedwetting, hemophilia A, von Willebrand disease, and high blood urea levels. [ 1] In hemophilia A and von Willebrand disease, it should only be used for mild to moderate cases. [ 1]
Wolfram syndrome, also called DIDMOAD ( d iabetes i nsipidus, d iabetes m ellitus, o ptic a trophy, and d eafness), is a rare autosomal-recessive genetic disorder that causes childhood-onset diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders including neurodegeneration.
Polyuria, nocturia, and polydipsia. Central diabetes insipidus, recently renamed arginine vasopressin deficiency (AVP-D), [ 1] is a form of diabetes insipidus that is due to a lack of vasopressin (ADH) production in the brain. Vasopressin acts to increase the volume of blood (intravascularly), and decrease the volume of urine produced.
Based on this clue, it soon came to light that there exist two types of hereditary diabetes insipidus. In 1947, the anti-diuretic hormone (ADH)-insensitive variety was termed nephrogenic diabetes insipidus (NDI), and attributed to a defect in the loop of Henle and the distal convoluted tubule. Since then, acquired forms of NDI have also been ...