Fanconi syndrome or Fanconi's syndrome (English: /fɑːnˈkoʊni/, /fæn-/) is a syndrome of inadequate reabsorption in the proximal renal tubules of the kidney...
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complementation groups. It should not be confused with Fanconi syndrome, a kidney disorder also named after Fanconi. FA is characterized by bone marrow failure,...
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Fanconi–Bickel syndrome is a form of glycogen storage disease named for Guido Fanconi and Horst Bickel, who first described it in 1949. It is associated...
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Cystinosis (redirect from Abderhalden–Kaufmann–Lignac syndrome)
body. Cystinosis is the most common cause of Fanconi syndrome in the pediatric age group. Fanconi syndrome occurs when the function of cells in renal tubules...
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Basenji (section Fanconi syndrome)
(incontinence, Fanconi syndrome, chronic kidney failure 13%), behavior ("unspecified" and aggression 9%), and cancer (9%). Fanconi syndrome, an inheritable...
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aminoaciduria and low-molecular-weight proteinuria. Lowe syndrome can be considered a cause of Fanconi syndrome (bicarbonaturia, renal tubular acidosis, potassium...
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affects the proximal renal tubules of the kidney. It is one cause of Fanconi syndrome, and is characterized by tubular proteinuria, excess calcium in the...
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anions inhibit mitochondrial DNA synthesis, it may cause iatrogenic Fanconi syndrome. The nucleoside phosphonate adefovir is a MRP2 inhibitor that has been...
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Organic anion transporter 1 (redirect from Iatrogenic Fanconi syndrome)
induced Fanconi syndrome. The use of stavudine, didenosine, abacavir, adefovir, cidofovir and tenofovir has been associated with Fanconi syndrome. Clinical...
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Prader–Willi syndrome (PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. In newborns, symptoms include weak...
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deletion syndrome 22q11.2 duplication syndrome 22q13 deletion syndrome 2p15-16.1 microdeletion syndrome 2q37 deletion syndrome 3-M syndrome 3C syndrome 3q29...
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Fanconi may refer to: Fanconi anemia, a genetic disease Fanconi syndrome, a kidney disease Guido Fanconi (1892–1979), a Swiss pediatrician This disambiguation...
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Fanconi anemia type 2 Fanconi anemia type 3 Fanconi–Bickel syndrome Fanconi ichthyosis dysmorphism Fanconi like syndrome Fanconi pancytopenia Fanconi...
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syndrome is named for Emil Abderhalden, Eduard Kaufmann and George Lignac. Renal Fanconi syndrome has sometimes been called Lignac–Fanconi syndrome,...
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reported for persons with mutations in TOP3A and RMI1. Bloom syndrome shares some features with Fanconi anemia possibly because there is overlap in the function...
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interstitial cystitis urinary tract infection renal tubular acidosis Fanconi syndrome nephronophthisis (genetic) Hormonal hypokalemia diabetes mellitus corticosteroid...
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(overflow proteinuria) Due to low reabsorption at proximal tubule (Fanconi syndrome) Proteinuria can also be caused by certain biological agents, such...
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extreme deterioration in kidney test results, which were consistent with Fanconi syndrome. Good Manufacture Practice (GMP) certification requires an external...
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Still's disease. It is named for Guido Fanconi and Hans Wissler It was first described by Wissler in 1944 and Fanconi in 1946. Single observations by E. Uhse...
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intrinsic problem with glucose reabsorption within the kidneys (such as Fanconi syndrome), producing a condition termed renal glycosuria. Glycosuria leads to...
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syndrome, Fanconi anemia, MUTYH-associated polyposis, Rothmund–Thomson syndrome, Werner syndrome and Xeroderma pigmentosum. Although cancer syndromes...
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Children with Down syndrome are susceptible to MDS, and a family history may indicate a hereditary form of sideroblastic anemia or Fanconi anemia. GATA2 deficiency...
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physicians including Fanconi Fanconi–Bickel syndrome Journal of Pediatrics. 96(4), p. 674 Who Named It? - Guido Fanconi Biography of Guido Fanconi by Stephan Lobitz...
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more generalised dysfunction of the proximal tubular cells called Fanconi syndrome where there is also phosphaturia, glycosuria, aminoaciduria, uricosuria...
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embryonically lethal condition; live cases usually experience a severe form of Fanconi anemia. A number of genes are associated with HBOC. The most common of...
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Hartnup disease (redirect from Hartnup syndrome)
differentiating it from other causes of generalized aminoaciduria, such as Fanconi syndrome. With urine chromatography, increased levels of neutral amino acids...
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Toni–Fanconi syndrome TORCH syndrome Toriello–Carey syndrome Toriello–Lacassie–Droste syndrome Toriello syndrome Toriello–Higgins–Miller syndrome Torres–Ayber...
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hypophosphatemia, hypoparathyroidism that is causing low blood calcium, and Fanconi syndrome. Vitamin-D supplements may not be effective in people with severe kidney...
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Renal tubular acidosis (redirect from Guibaud Vainsel syndrome)
more generalized dysfunction of the proximal tubular cells called Fanconi syndrome, in which there is also phosphaturia, glycosuria, aminoaciduria, uricosuria...
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retardation Lactic acidosis Renal Fanconi syndrome Other symptoms that happen in a smaller percentage of people with GRACILE syndrome include: Death in early adulthood...
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