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Fanconi syndrome or Fanconi's syndrome (English: / f ɑː n ˈ k oʊ n i /, / f æ n-/) is a syndrome of inadequate reabsorption in the proximal renal tubules [1] of the kidney. The syndrome can be caused by various underlying congenital or acquired diseases, by toxicity (for example, from toxic heavy metals), or by adverse drug reactions. [2]
28 Σεπ 2022 · Fanconi syndrome is a condition that affects how your kidneys reabsorb minerals and nutrients that you need to function. It’s a rare condition, and you may inherit faulty genes from your biological parents that cause it.
4 Ιουλ 2023 · Fanconi syndrome, not to be confused with Fanconi anemia, is a defect of the proximal tubule that prevents the absorption of electrolytes and other substances that are normally absorbed by the proximal tubule. Fanconi syndrome can occur as an inherited or acquired condition.
27 Αυγ 2019 · Fanconi syndrome (FS) is a rare disorder that affects the filtering tubes (proximal tubules) of the kidney. Learn more about the different parts of the kidney and see a diagram here.
Fanconi syndrome consists of multiple defects in renal proximal tubular reabsorption, causing glucosuria, phosphaturia, generalized aminoaciduria, and bicarbonate wasting. It may be hereditary or acquired.
Fanconi syndrome is a rare disorder of kidney tubule function that results in excess amounts of glucose, bicarbonate, phosphates (phosphorus salts), uric acid, potassium, and certain amino acids being excreted in the urine.
Fanconi syndrome consists of multiple defects in renal proximal tubular reabsorption , causing glucosuria, phosphaturia, generalized aminoaciduria, and bicarbonate wasting. It may be hereditary or acquired. Symptoms in children are failure to thrive, growth retardation, and rickets. Symptoms in adults are osteomalacia and muscle weakness.
Fanconi syndrome, also known as the DeToni, Debré, Fanconi syndrome is a global dysfunction of the proximal tubule characterized by glucosuria, phosphaturia, generalized aminoaciduria, and type II renal tubular acidosis. Often there is hypokalemia, sodium wasting, and dehydration.
16 Σεπ 2022 · Fanconi syndrome (FS) is a systemic proximal tubular dysfunction characterized by proteinuria, glycosuria, phosphateuria, generalized hyperaminoaciduria, hypokalemia, hypophosphatemia, and type II renal tubular acidosis . Fanconi syndrome can be triggered by different causes, including hereditary, idiopathic, and acquired.
4 Ιουλ 2023 · Fanconi syndrome is a defect of proximal tubule leading to malabsorption of various electrolytes and substances that are usually absorbed by the proximal tubule. It could be an inherited or acquired condition.
