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Xu, C. Hyperlysinemia. Encyclopedia. Available online: https://encyclopedia.pub/entry/4134 (accessed on 28 September 2026).
Xu C. Hyperlysinemia. Encyclopedia. Available at: https://encyclopedia.pub/entry/4134. Accessed September 28, 2026.
Xu, Camila. "Hyperlysinemia" Encyclopedia, https://encyclopedia.pub/entry/4134 (accessed September 28, 2026).
Xu, C. (2020, December 23). Hyperlysinemia. In Encyclopedia. https://encyclopedia.pub/entry/4134
Xu, Camila. "Hyperlysinemia." Encyclopedia. Web. 23 December, 2020.
Hyperlysinemia
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/hyperlysinemia

Hyperlysinemia is an inherited condition characterized by elevated blood levels of the amino acid lysine, a building block of most proteins.

genetic conditions

References

  1. Markovitz PJ, Chuang DT, Cox RP. Familial hyperlysinemias. Purification andcharacterization of the bifunctional aminoadipic semialdehyde synthase withlysine-ketoglutarate reductase and saccharopine dehydrogenase activities. J Biol Chem. 1984 Oct 10;259(19):11643-6.
  2. Sacksteder KA, Biery BJ, Morrell JC, Goodman BK, Geisbrecht BV, Cox RP, Gould SJ, Geraghty MT. Identification of the alpha-aminoadipic semialdehyde synthasegene, which is defective in familial hyperlysinemia. Am J Hum Genet. 2000Jun;66(6):1736-43.
  3. Saudubray JM, Rabier D. Biomarkers identified in inborn errors for lysine,arginine, and ornithine. J Nutr. 2007 Jun;137(6 Suppl 2):1669S-1672S. doi:10.1093/jn/137.6.1669S. 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: 808
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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