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hypophosphatemia
Hypophosphatemia Washington Manual of Medical Therapeutics.
Hypophosphatemia may also occur from osmotic diuresis and disorders of proximal tubular transport such as familial X-linked hypophosphatemic rickets and Fanconi syndrome. In acutely ill patients on continuous renal replacement therapy, the removal of phosphorous by slow continuous dialysis can also result in hypophosphatemia.
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Incidence of Hypophosphatemia After Treatment With Iron Isomaltoside/Ferric Derisomaltose or Ferric Carboxymaltose in Subjects With Iron Deficiency Anaemia Full Text View ClinicalTrials.gov.
Evaluate the proportion of subjects with hypophosphatemia s-phosphate level 2.0 mg/dL on day 35. Absolute Changes in S-phosphate From Baseline to Day 1, 7, 8, 14, 21, and 35 Time Frame: Baseline, days 1, 7, 8, 14, 21, and 35.
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Burosumab Therapy in Children with X-Linked Hypophosphatemia NEJM. logo-32. logo-40. logo-60. New England Journal of Medicine.
X-linked hypophosphatemia, a disorder of renal phosphate wasting and the most common heritable form of rickets, is caused by loss-of-function mutations in the gene encoding phosphate-regulating endopeptidase homolog X-linked PHEX, which results in excess circulating fibroblast growth factor 23 FGF-23.
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A Unique Case of Hypophosphatemia in the Setting of Oliguric Acute Kidney Injury.
Hypophosphatemia; Acute kidney injury; Refeeding syndrome. Hypophosphatemia is a frequently encountered electrolyte disorder in critically ill patients with acute kidney injury AKI and usually occurs in the background of renal replacement therapy 1. It is associated with high mortality in these patients.
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X-linked Hypophosphatemia XLH, a Rare Genetic Disorder XLHLink.
Hereditary, progressive, and lifelong. XLH, or X-linked hypophosphatemia, is a condition that affects bones, muscles, and teeth due to the excessive loss of phosphate. Phosphate is lost through the urine, which causes low levels of phosphorus in the blood, a condition called phosphate wasting or hypophosphatemia.
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hypophosphatemia Wiktionary.
hypophosphatemia countable and uncountable, plural hypophosphatemias. English Wikipedia has an article on.: medicine An electrolyte disturbance in which there is an abnormally low level of phosphate in the blood, most commonly seen when malnourished patients are given large amounts of carbohydrates, creating a high phosphorus demand in the cells of the body.
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Severe Hypophosphatemia in a Patient with Acute Pancreatitis Insight Medical Publishing.
Even though the role of the alcohol-induced renal phosphate wasting is of paramount importance, the marked hypophosphatemia observed on the second day of hospitalization could be the result of the increased transfer of phosphate from the extracellular to the intracellular fluid.
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GeneDx.
In contrast, Pseudovitamin D-deficiency rickets is an autosomal recessive condition due to mutations in the CYP27B1 gene and is responsive to treatment with Vitamin D. Another autosomal recessive form of rickets characterized by hypophosphatemia and osteomalacia, which is phenotypically similar to the more common X-linked form but is responsive to treatment with phosphate and vitamin D substitution, is caused by mutations in the DMP1 gene.
Hypophosphatemia: Background, Pathophysiology, Epidemiology. Group 2. 34A8E98B-62ED-4216-98D6-E986304F4C2E.
Acute severe hypophosphatemia can manifest as widespread organ dysfunction. Hypophosphatemia in the ICU setting is associated with respiratory insufficiency due to impaired diaphragmatic contractility and depressed cardiac output due to decreased myocardial contractility that reverse with correction of the electrolyte abnormality.

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