(hi″pәr-li″se-ne´me-ә) a congenital type of aminoacidopathy characterized by elevated levels of lysine in the blood, and marked by vomiting, spasticity, coma, and mental retardation; symptoms are related to protein intake.
Found on http://www.encyclo.co.uk/local/21001
Type: Term Pronunciation: hī′pĕr-lī′si-nē′mē-ă Definitions: 1. A metabolic disorder characterized by mental retardation, convulsions, anemia, and asthenia; associated with an abnormal increase of the amino acid lysine in the circulating blood due to a deficiency of lysine-ketoglutarate reductase. One
Found on http://www.medilexicon.com/medicaldictionary.php?t=42440
Hyperlysinemia is an autosomal recessive metabolic disorder characterized by an abnormal increase of lysine in the blood, but appears to be benign. It is caused by mutations in AASS, which encodes α-aminoadipic semialdehyde synthase. == Genetics == Hyperlysinemia is inherited in an autosomal recessive manner. This means the defective gene respons
Found on http://en.wikipedia.org/wiki/Hyperlysinemia
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