Results 21 to 30 of about 26,759 (219)
Transient Antenatal Bartter’s Syndrome: A Case Report
Frontiers in Pediatrics, 2018 Antenatal Bartter’s syndrome is a rare inherited disorder characterized by fetal polyhydramnios and polyuria that is usually detected between 24 and 30 weeks of gestation. However, a rare, severe, but transient form of antenatal Bartter’s syndrome due to
Michelle Meyer +2 more
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Effect of T3 Spinal Contusion Injury on Upper Urinary Tract Function
Neurotrauma Reports, 2022 Spinal cord injury (SCI) significantly impacts many systems attributable to disrupted autonomic regulation of the body. Of these disruptions, excessive production/passage of urine (polyuria) has been understudied.
Jason H. Gumbel, Charles H. Hubscher
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Transient central diabetes insipidus following ischemic stroke
Indian Journal of Endocrinology and Metabolism, 2013 Central Diabetes Insipidus (CDI) following ischemic infarction of the brain has been described as a rare presentation. Posterior pituitary ischemia has also been postulated as a possible cause of idiopathic CDI. We encountered a young male with bilateral
Muthukrishnan Jayaraman +2 more
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Familial Hypomagnesemia With Hypercalciuria and Nephrocalcinosis in a 7-Year-Old Girl: A Case Report. [PDF]
Clin Case RepABSTRACT Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare autosomal recessive renal tubular disorder, caused by mutations in the Claudin‐16 or Claudin‐19 genes. It is characterized by renal wasting of calcium and magnesium, bilateral nephrocalcinosis, and progression to kidney failure eventually.
Tonny RT, Mumu FA, Sharmim S, Huque SS.
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Insipidary syndrome in children and adolescents (part 2)
Лечащий Врач, 2021 The review article presents current data on water-electrolyte balance in healthy and pathological state. The diseases and conditions which occur in insipidary syndrome are described.
V. V. Smirnov, L. I. Bikbaeva
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Metabolites, 2022 (1) Background: Evidence has accumulated regarding the etiology of lower urinary tract symptoms associated with obesity and metabolic syndrome. Therefore, the present study aimed to identify which subjectively and objectively measured voiding parameters ...
Asuka Ashikari +11 more
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Bartter Syndrome Presenting with Metabolic Alkalosis: A Case Series [PDF]
Journal of Clinical and Diagnostic Research, 2023 Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochloraemic metabolic alkalosis. Children present with the complaint of polyuria, dehydration, failure to thrive and normal blood pressure despite ...
Gulam Mohammed
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Nocturnal Urine Production in Women With Global Polyuria [PDF]
International Neurourology Journal, 2020 Purpose Low nocturnal urine production (NUP) may be sufficient to rule out global polyuria (GP) in men. This study determines the sensitivity of indices for nocturnal polyuria (NP), defined as nocturnal polyuria index (NPi; nocturnal urine volume/24-hour
Thomas F. Monaghan +13 more
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Poiseuille’s law in polyuria [PDF]
Pediatric Nephrology, 2014 Dear Sir,In their recent paper, Caletti et al. describe urinary tract find-ings in children with nephrogenic diabetes insipidus (NDI)and show that seven out of ten patients have renal pelvicdilatation that improved or even normalized during follow-up[1].Treatmentwithalowosmolardietincombinationwithdiuretics and indomethacin reduced the urine output ...
Schreuder, M.F., Koster-Kamphuis, L.
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Central Diabetes Insipidus in Acute Myeloid Leukemia with Cytogenetic Abnormality of 9q34 Deletion
Oman Medical JournalAcute 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
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