Diabetes mellitus remission in a cat with pituitary-dependent hyperadrenocorticism after trilostane treatment [PDF]
, 2018 An 8-year-old male neutered Persian cat was presented with polyuria, polydipsia, polyphagia and muscle weakness associated with a 7 month history of diabetes mellitus (DM).
Adriana Cunha Muschner +4 more
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A Rare Case of Familial Neurogenic Diabetes Insipidus in a 22-Year-Old Man
AACE Clinical Case Reports, 2021 Objective: Diabetes insipidus (DI) can be classified into 2 types: central/neurogenic DI and nephrogenic DI. Most cases of central DI occur after brain surgery, trauma, tumor, or infection.
Van T.T. Phan, MD +4 more
doaj
Persistent isolated hypocortisolism following brief treatment with trilostane [PDF]
, 2008 A 12-year-old male neutered Miniature Poodle with confirmed pituitary-dependent hyperadrenocorticism was treated with trilostane. After three doses, it developed clinical and laboratory changes suggestive of isolated hypocortisolism ('atypical ...
Barker +19 more
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Central diabetes insipidus in a young dog - case report [PDF]
Arquivo Brasileiro de Medicina Veterinária e ZootecniaThis work reports a case of an 11-month-old spayed, female mongrel with polyuria, polydipsia, polakiuria and nocturia. Serum biochemistry (alkaline phosphatase, ALT, urea, creatinine, GGT, globulins, triglycerides, cholesterol, total proteins), hemogram,
R.R. Ribeiro +3 more
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Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: A case report [PDF]
, 2018 Background: Sixty mutations of claudin 16 coding gene have been reported in familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) patients. Recent investigations revealed that a highly conserved glycine-leucine-tryptophan (115G-L-W117)
Bottillo, I +5 more
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EJE AWARD 2019: New diagnostic approaches for patients with polyuria polydipsia syndrome
European Journal of Endocrinology, 2019 Diabetes insipidus (DI), be it from central or nephrogenic origin, must be differentiated from secondary forms of hypotonic polyuria such as primary polydipsia. Differentiation is crucial since wrong treatment can have deleterious consequences.
M. Christ-Crain
semanticscholar +1 more source
Effects of desmopressin acetate administration in healthy dogs receiving prednisolone
Journal of Veterinary Internal Medicine, 2021 Background Glucocorticoids are used for a variety of purposes in veterinary medicine but often are associated with clinically important adverse effects. Polyuria and polydipsia are the most frustrating adverse effects noted by owners.
Pamela Galati +5 more
doaj +1 more source
Recurrent Hyponatremia in the Setting of Autoimmune Disease with Sicca Syndrome: A Case Report
Case Reports in Nephrology and Dialysis, 2023 Sjogren’s syndrome is an autoimmune disease associated with xerostomia and xerophthalmia. The association of Sjogren’s with hyponatremia has rarely been reported and has been attributed to syndrome of inappropriate antidiuretic hormone secretion.
Ahmad El-Moussa +4 more
doaj +1 more source
Journal of Clinical Endocrinology and Metabolism, 2015 CONTEXT The polyuria-polydipsia syndrome comprises primary polydipsia (PP) and central and nephrogenic diabetes insipidus (DI). Correctly discriminating these entities is mandatory, given that inadequate treatment causes serious complications.
K. Timper +11 more
semanticscholar +1 more source
Psychogenic polidipsia in a patient with bipolar affective disorder (BAD)
European Psychiatry, 2021 Introduction A 49 y.o. male patient was admitted to the male PICU with a manic episode. Upon admission he presented with mood elation, pressured speech, lack of sleep, agitation and polydipsia.
A. Sarafopoulos +2 more
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