(hi-drok″se-pro″lĭ-ne´me-ә) an autosomal recessive aminoacidopathy characterized by an excess of free hydroxyproline in the plasma and urine, due to a defect in the enzyme hydroxyproline oxidase.
Found on
http://www.encyclo.co.uk/local/21001
Type: Term Pronunciation: hī-drok′sē-prō′li-nē′mē-ă Definitions: 1. A metabolic disorder characterized by mental retardation and microscopic hematuria in some patients; associated with enhanced plasma concentration and urinary excretion of free hydroxyproline because of a deficiency of hydroxyproline ...
Found on
http://www.medilexicon.com/medicaldictionary.php?t=42109
No exact match found.
