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Diabetes insipidus ( DI ), alternately called arginine vasopressin deficiency (AVP-D) or arginine vasopressin resistance (AVP-R), [5] is a condition characterized by large amounts of dilute urine and increased thirst. [1] The amount of urine produced can be nearly 20 liters per day. [1] Reduction of fluid has little effect on the concentration ...
Nephrogenic diabetes insipidus. Nephrogenic diabetes insipidus, recently renamed arginine vasopressin resistance (AVP-R) and previously known as renal diabetes insipidus, is a form of diabetes insipidus primarily due to pathology of the kidney. This is in contrast to central or neurogenic diabetes insipidus, which is caused by insufficient ...
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.
What is diabetes insipidus? You’re no doubt aware of diabetes mellitus, which has type 1 and type 2 variations. It’s a disorder of water balance and control in the body, explains Christopher ...
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. [2] [3] [4]
Types of diabetes insipidus. Since about 1850 it had been known that diabetes insipidus might be a hereditary disorder. In 1945, it was noted that vasopressin had no effect on treating some patients with familial diabetes. Based on this clue, it soon came to light that there exist two types of hereditary diabetes insipidus.
A condition in which the immune system inappropriately attacks a body tissue. Multiple sclerosis, some kinds of rheumatism, lupus, and Type 1 diabetes are examples. The reasons for the immune system misbehavior are not, in general, understood. Damage to nerves that do not control senses or muscles.
As a diagnosis of exclusion, a diagnosis of primary polydipsia may be the result of elimination of the possibility of diseases causing similar signs and symptoms, such as diabetes insipidus. Diagnosis may be complicated by the fact that chronic and extreme compulsive drinking may impair the response of the kidneys to vasopressin, thus reducing ...
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