Hyperlysinemia

Hyperlysinemia is an autosomal recessive metabolic disorder characterized by an abnormal increase of lysine in the blood, but appears to be benign. It can be associated with saccharopine dehydrogenase. == Genetics == Hyperlysinemia is inherited in an autosomal recessive manner. This means the defective gene responsible for the disorder is located
Found on http://en.wikipedia.org/wiki/Hyperlysinemia

hyperlysinemia

(hi″pәr-li″se-neĀ“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

hyperlysinemia

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
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