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词条 Hexokinase deficiency
释义

  1. See also

  2. References

  3. External links

{{Infobox medical condition (new)
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}}Hexokinase deficiency is an anemia-causing condition associated with inadequate hexokinase.[1][2] Specifically, the HK1 isozyme is involved.[3]

An acronym for Hexokinase deficiency is HK deficiency, and it is a genetic disease. The person must be homozygous for the trait, as being heterozygous would just make the person a carrier of that mutated gene.[4]

The cause of hexokinase deficiency is linked to mutations of the HK gene and the encoding of the HK enzyme. The result of the mutations lead to reduction in HK activity.[4]

See also

  • List of hematologic conditions

References

1. ^{{cite web|url=http://dwb.unl.edu/teacher/nsf/c10/c10links/www.emory.edu/INT_MED_REV/Atlanta/paper/paper.htm |title=DISORDERS OF RED CELLS |work= |accessdate=2009-02-07 |deadurl=yes |archiveurl=https://web.archive.org/web/20070826233455/http://dwb.unl.edu/Teacher/NSF/C10/C10Links/www.emory.edu/INT_MED_REV/Atlanta/paper/paper.htm |archivedate=2007-08-26 |df= }}
2. ^{{cite journal |vauthors=Paglia DE, Shende A, Lanzkowsky P, Valentine WN |title=Hexokinase "New Hyde Park": a low activity erythrocyte isozyme in a Chinese kindred |journal=Am. J. Hematol. |volume=10 |issue=2 |pages=107–17 |year=1981 |pmid=7234862 |doi= 10.1002/ajh.2830100202|url=}}
3. ^{{OMIM|235700}}
4. ^{{cite web|title=Hexokinase deficiency|url=http://www.enerca.org/anaemias/38/hexokinase-deficiency|website=www.enerca.org|publisher=European Network for Rare and Congenital Anaemias|accessdate=April 6, 2017}}

External links

{{Medical resources
| DiseasesDB =
| ICD10 = {{ICD10|D|55|2|d|55}}
| ICD9 = {{ICD9|282.3}}
| ICDO =
| OMIM = 235700
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}}{{Diseases of RBCs}}{{Inborn errors of carbohydrate metabolism}}

2 : Hereditary hemolytic anemias|Inborn errors of carbohydrate metabolism

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