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Xu, C. Histidinemia. Encyclopedia. Available online: https://encyclopedia.pub/entry/4111 (accessed on 26 September 2026).
Xu C. Histidinemia. Encyclopedia. Available at: https://encyclopedia.pub/entry/4111. Accessed September 26, 2026.
Xu, Camila. "Histidinemia" Encyclopedia, https://encyclopedia.pub/entry/4111 (accessed September 26, 2026).
Xu, C. (2020, December 23). Histidinemia. In Encyclopedia. https://encyclopedia.pub/entry/4111
Xu, Camila. "Histidinemia." Encyclopedia. Web. 23 December, 2020.
Histidinemia
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/histidinemia

Histidinemia is an inherited condition characterized by elevated blood levels of the amino acid histidine, a building block of most proteins. Histidinemia is caused by the shortage (deficiency) of the enzyme that breaks down histidine. Histidinemia typically causes no health problems, and most people with elevated histidine levels are unaware that they have this condition.

genetic conditions

References

  1. Kawai Y, Moriyama A, Asai K, Coleman-Campbell CM, Sumi S, Morishita H, SuchiM. Molecular characterization of histidinemia: identification of four missensemutations in the histidase gene. Hum Genet. 2005 Apr;116(5):340-6.
  2. Taylor RG, Levy HL, McInnes RR. Histidase and histidinemia. Clinical andmolecular considerations. Mol Biol Med. 1991 Feb;8(1):101-16. Review.
  3. Virmani K, Widhalm K. Histidinemia: a biochemical variant or a disease? J AmColl Nutr. 1993 Apr;12(2):115-24. Review.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Camila Xu
View Times: 1.0K
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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