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Imerslund-Gräsbeck syndrome
Imerslund-Grasbeck syndrome or Imerslund-Najman-Grasbeck syndrome or Imerslund-Grasbeck disease (IGS or INGS) is an autosomal recessive, familial form ...
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Imerslund-Gräsbeck syndrome (IGS) or selective vitamin B12 (cobalamin) malabsorption with proteinuria is a rare autosomal recessive disorder characterized ...
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A US Department of Health and Human Service project providing information on genetic and rare diseases. A comprehensive body of resources on ...
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J Pediatr Hematol Oncol. 2006 Nov;28(11):715-9. Imerslund-Grasbeck syndrome associated with recurrent aphthous stomatitis and defective neutrophil function.
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Keywords: Megaloblas c anemia, Imerslund-Grasbeck Syndrome, Proteinuria. Introduction. Megaloblas c anemia is an uncommon problem in childhood most ...
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Imerslund-Grasbeck syndrome (IGS) is caused by a defective transport of cobalamin by enterocytes. it is characterized by prominent megaloblastic anemia and ...
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Aug 26, 2011 ... The Imerslund-Grasbeck syndrome of proteinuria and excretion of cobalamin and IF is a rare disorder that arises in early childhood. However ...
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To present a case thought to be Imerslund-Grasbeck syndrome because of vitamin B12 deficiency, proteinuria and glossitis. A 5-year-old girl presented at our ...
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Imerslund-Grasbeck Syndrome. Guner Karatekin, Betul Sezgin*, Semra Kayaoglu, Asiye Nuhoglu. From the Department of Pediatrics, Sisli Etfal Hospital, ...
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Dec 19, 2011 ... Recently, scientists discovered an ancient mutant gene putting vitamin B12 deficiency around the timeline of 11600 B.C., causing a rare form of ...
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