different between homocysteine vs homocystinuria

English

Etymology

homo- +? cysteine.

Noun

homocysteine (countable and uncountable, plural homocysteines)

1. (biochemistry) An amino acid which is monitored in the blood to estimate risk of cardiovascular disease.
   • 1989, L. A. Smolin, N. A. Benevenga, Chapter 8: Methionine, Homocyst(e)ine, Cysteine—Metabolic Interrelationships, Mendel Friedman, Absorption and Utilization of Amino Acids, Volume 1, CRC Press, page 170,

     One possible explanation for the low plasma cystine in homocystinuric patients who are given sufficient dietary cystine is the high plasma concentration of the cysteine-homocysteine mixed disulfide.

   • 2000, Donald W. Jacobsen, 3. Biochemistry and Metabolism, Killian Robinson (editor), Homocysteine and Vascular Disease, Kluwer Academic, page 15,

     Homocysteine, a metabolite of the methionine cycle, is a strong independent risk factor for cardiovascular disease.

   • 2017, Himadri Panda, Handbook on Small & Medium Scale Industries (Biotechnology Products), Asia Pacific Business Press, page 224,

     The amino acids produced from L-methionine and substituted thiols were identified as the corresponding S-substituted homocysteines, e.g., 2-mercaptoethanol and cysteamine produced S-(?-hydroxyethyl) homocysteine and S-(?-aminoethyl) homocysteine, respectively.

Usage notes

Not to be confused with homocystine (a different compound whose relationship with homocysteine is analogous to that of cystine with cysteine).

Derived terms

• homocysteinemia
• homocystinuria
• hyperhomocysteinemia

See also

• homocystine

English

Noun

homocystinuria (countable and uncountable, plural homocystinurias)

1. (medicine) An inherited metabolic disorder characterised by the presence of homocysteine in the urine

Related terms

• homocystinuric

Translations