KEGG   DISEASE: ビタミン B12 欠乏性貧血
エントリ  
H01277                                                             
名称    
ビタミン B12 欠乏性貧血
  下位グループ
Imerslund-Grasbeck 症候群 (IGS)
遺伝性内因子欠損症 (IFD)
概要    
Vitamin B12 deficiency anaemia is caused by intestinal malabsorption of cobalamin. Imerslund-Grasbeck syndrome (IGS) is an autosomal recessive disorder characterized by juvenile megaloblastic anaemia and neurological symptoms such as peripheral neuropathy, cognitive problems, and dementia. If untreated, the disease is fatal. Biallelic mutations either in the cubilin (CUBN) or amnionless (AMN) gene cause IGS. Both proteins are involved in intestinal absorption and renal tubular reabsorption. Hereditary intrinsic factor deficiency (IFD) is a phenotype that is caused by mutations in CBLIF, the gene encoding intrinsic factor.
カテゴリ  
血液疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 03 血液・造血器の疾患
  貧血または他の赤血球系疾患
   栄養性または代謝性の貧血
    3A01  ビタミンB12欠乏による巨赤芽球性貧血
     H01277  ビタミン B12 欠乏性貧血
パスウェイに基づく疾患分類 [BR:jp08402]
 補因子・ビタミン代謝
  nt06538  コバラミンの輸送と代謝
   H01277  ビタミン B12 欠乏性貧血
パスウェイ 
hsa04977  Vitamin digestion and absorption
ネットワーク
nt06538 Cobalamin transport and metabolism
病因遺伝子 
(IGS1) CUBN [HSA:8029] [KO:K14616]
(IGS2) AMN [HSA:81693] [KO:K18259]
(IFD) CBLIF [HSA:2694] [KO:K14615]
リンク   
ICD-11: 3A01
MeSH: C563242
OMIM: 261100 618882 261000
文献    
  著者
Grasbeck R
  タイトル
Imerslund-Grasbeck syndrome (selective vitamin B(12) malabsorption with proteinuria).
  雑誌
Orphanet J Rare Dis 1:17 (2006)
DOI:10.1186/1750-1172-1-17
文献    
PMID:10080186 (CUBN)
  著者
Aminoff M, Carter JE, Chadwick RB, Johnson C, Grasbeck R, Abdelaal MA, Broch H, Jenner LB, Verroust PJ, Moestrup SK, de la Chapelle A, Krahe R
  タイトル
Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1.
  雑誌
Nat Genet 21:309-13 (1999)
DOI:10.1038/6831
文献    
PMID:24044590 (AMN)
  著者
De Filippo G, Rendina D, Rocco V, Esposito T, Gianfrancesco F, Strazzullo P
  タイトル
Imerslund-Grasbeck syndrome in a 25-month-old Italian girl caused by a homozygous mutation in AMN.
  雑誌
Ital J Pediatr 39:58 (2013)
DOI:10.1186/1824-7288-39-58
文献    
PMID:15738392 (CBLIF)
  著者
Tanner SM, Li Z, Perko JD, Oner C, Cetin M, Altay C, Yurtsever Z, David KL, Faivre L, Ismail EA, Grasbeck R, de la Chapelle A
  タイトル
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.
  雑誌
Proc Natl Acad Sci U S A 102:4130-3 (2005)
DOI:10.1073/pnas.0500517102
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