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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 ...
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]
A pregnant woman experiences stomach pains and headaches; another woman experiences eye inflammation and joint stiffness. 32. 5. "The Purple Puzzle". December 10, 2007. ( 2007-12-10) An abnormality on the ultrasound alarms parents expecting a baby; a biology teacher has a series of strange symptoms. 33. 6.
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 ...
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.
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 ...
The triad of diabetes insipidus, exophthalmos, and lytic bone lesions is known as the Hand-Schüller-Christian triad. Peak onset is 2–10 years of age. Multifocal multisystem. Multifocal multisystem LCH, also called Letterer-Siwe disease, is an often rapidly progressing disease in which Langerhans Cell cells proliferate in many tissues. It is ...
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.
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