homocystinemia

ho·mo·cys·ti·ne·mi·a

(hō'mō-sis'ti-nē'mē-ă),
Presence of an excess of homocystine in the plasma, as in homocystinuria.

homocystinemia

[-sis′tinē′mē·ə]
an amino acid disorder that causes an excess of homocystine in the blood. See also homocystinuria.

ho·mo·cys·ti·ne·mi·a

(hō'mō-sis'ti-nē'mē-ă)
Presence of an excess of homocystine in the plasma, as in homocystinuria.
Synonym(s): homocystinaemia.
References in periodicals archive ?
Cobalamin C (cblC) disease is the most common type of MMA and is characteristically concurrent with homocystinemia (HCY) due to impaired synthesis of two active forms of cbl, namely adenosylcobalamin (AdoCbl) and methylcobalamin (MeCbl).
Microspherophakia is usually associated with systemic disorders such as Weill-Marchesani syndrome (WMS), homocystinemia, Marfan syndrome, Alport syndrome and Klinefelter syndrome.
Homocystinemia as an independent risk factor in the Chinese population at a high risk of coronary artery disease.
Homocystinemia does not appear to be a risk factor solely for ischemic heart disease either.