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Imerslund-Grasbeck syndrome

An autosomal recessive congenital form of megaloblastic anemia due to vitamin B12 deficiency; proteinuria is also present. The disorder is caused by a defect in the vitamin B12/intrinsic factor receptor (CUBN gene mutation). Mutations in the AMN gene have also been identified. OMIM: 261100
Also Known As:
Enterocyte cobalamin malabsorption; Enterocyte intrinsic factor receptor, defect of; Megaloblastic Anemia 1
Networked: 19 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Related Diseases

1. Proteinuria
2. Megaloblastic Anemia
3. Vitamin B 12 Deficiency (Vitamin B12 Deficiency)
4. Pernicious Anemia
5. Intrinsic Factor Deficiency

Experts

1. Tanner, Stephan M: 4 articles (11/2006 - 03/2003)
2. de la Chapelle, Albert: 3 articles (03/2005 - 03/2003)
3. Altay, Cigdem: 2 articles (11/2005 - 03/2005)
4. Cetin, Mualla: 2 articles (11/2005 - 03/2005)
5. Gräsbeck, Ralph: 2 articles (03/2005 - 05/2003)
6. Fyfe, John C: 2 articles (03/2004 - 11/2003)
7. He, Qianchuan: 2 articles (03/2004 - 11/2003)
8. Aminoff, Maria: 2 articles (05/2003 - 03/2003)
9. Banka, Siddharth: 1 article (09/2019)
10. Ciancio, Jose I R: 1 article (09/2019)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Imerslund-Grasbeck syndrome:
1. Vitamin B 12 (Cyanocobalamin)FDA LinkGeneric
2. Intrinsic FactorFDA Link
3. intrinsic factor-cobalamin receptorIBA
4. VitaminsIBA
5. Transcobalamins (Transcobalamin II)IBA
6. Phenobarbital (Luminal)FDA Link