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Central and nephrogenic diabetes insipidus: updates on diagnosis and management [PDF]

open access: yesFrontiers in Endocrinology
Diabetes insipidus (DI) is a rare endocrine disease involving antidiuretic hormone (ADH), encompassing both central and nephrogenic causes. Inability to respond to or produce ADH leads to inability of the kidneys to reabsorb water, resulting in hypotonic
Kathryn Flynn   +4 more
doaj   +2 more sources

Polydipsia, Psychosis, and Familial Psychopathology [PDF]

open access: bronzeThe Canadian Journal of Psychiatry, 2001
Objective: To compare the demographic and clinical factors and familial psychopathology of chronic psychiatric inpatients with, and without, polydipsia. Method: We undertook a case-control study of chronic psychiatric inpatients both with, and without, polydipsia.
AG Ahmed, Liana M Heigh, KV Ramachandran
openalex   +4 more sources

Central Diabetes Insipidus in Acute Myeloid Leukemia with Cytogenetic Abnormality of 9q34 Deletion [PDF]

open access: yesOman Medical Journal
Acute myeloid leukemia (AML) is rarely associated with central diabetes insipidus (CDI) with unclear underlying pathophysiological mechanisms. The most commonly reported cytogenetic abnormality in cases of AML-associated CDI is monosomy 7, followed by ...
Majd Farajallah   +3 more
doaj   +2 more sources

Knowledge of Psychogenic Polydipsia Within Mental Health Services [PDF]

open access: yesBJPsych Open
Aims Psychogenic polydipsia (PP) is a term used to describe a repetitive behaviour that characterises compulsivity in psychiatric patients resulting in excessive fluid consumption.
Ewelina De Leon   +2 more
doaj   +2 more sources

Desmopressin responding female nephrogenic diabetes insipidus: a case report [PDF]

open access: yesChildhood Kidney Diseases, 2022
Nephrogenic diabetes insipidus, decreased ability to concentrate urine, with production of large amounts of urine, is caused by the refractory response of renal tubules to the action of antidiuretic hormone.
Juyeon Lee   +3 more
doaj   +1 more source

Polydipsia and autistic traits in patients with schizophrenia spectrum disorders

open access: yesFrontiers in Psychiatry, 2023
IntroductionPolydipsia, prevalent in 6%–20% of patients with schizophrenia, results in seclusion and prolonged hospitalization. It is also observed in autistic individuals, with previous studies reporting that autism accounted for 20% of all hospitalized
Hiroshi Komatsu   +13 more
doaj   +1 more source

A 14-year-old male with rhabdomyolysis associated with psychogenic polydipsia and hyponatremia [PDF]

open access: yesPediatric Emergency Medicine Journal, 2023
Rhabdomyolysis associated with psychogenic polydipsia and hyponatremia is a rare condition that can cause substantial morbidity and mortality. We report a 14-year-old boy with psychogenic polydipsia who experienced recurrent hyponatremia and subsequent ...
Youn Shin Jung   +5 more
doaj   +1 more source

Biallelic GTF2IRD1 variants in brothers with profound neurodevelopmental disorder: A possible novel disorder involving a critical gene for Williams syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 191, Issue 2, Page 332-337, February 2023., 2023
Abstract GTF2IRD1, a gene on chromosome 7 which encodes a transcription factor, is of significant clinical interest due to its heterozygous loss as part of the classical deletion associated with Williams–Beuren syndrome (WBS). However, biallelic variants in GTF2IRD1 alone as part of an autosomal recessive disease have not been previously reported. Here,
Christopher Thomas Cummings   +1 more
wiley   +1 more source

Pagophagia-Induced Hyponatremia: An Unusual Case

open access: yesSudan Journal of Medical Sciences, 2023
Hyponatremia occurs when the serum sodium level is below 135 mmol/L. The symptoms include nausea, vomiting, confusion, headache, cardiorespiratory symptoms, profound somnolence or coma, and seizures are observed.
Aydanur Akbaba   +4 more
doaj   +1 more source

Systemic calcinosis in a Quarter Horse gelding homozygous for a myosin heavy chain 1 mutation

open access: yesJournal of Veterinary Internal Medicine, 2022
Case Description A 9‐year‐old Quarter Horse gelding was presented for lethargy, decreased appetite, polyuria and polydipsia (PU/PD), and severe muscle wasting suggestive of immune‐mediated myositis.
Beatrice T. Sponseller   +5 more
doaj   +1 more source

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