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hyperglycinemia hy·per·gly·ci·ne·mi·a (hī’pər-glī’sə-nē’mē-ə)
A hereditary disorder marked by an elevated concentration of glycine in the blood, usually present within chylomicrons.


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  • Hyperglycinemia with hyperglycinuria

    hyperglycinemia with hyperglycinuria n. A hereditary, usually fatal metabolic disorder generally appearing shortly after birth and characterized by vomiting, metabolic acidosis, ketonuria, osteoporosis, periodic thrombocytopenia, neutropenia, mental retardation, and neuropsychiatric dysfunction. Also called glycinemia.

  • Hyperglycogenolysis

    hyperglycogenolysis hy·per·gly·co·gen·ol·y·sis (hī’pər-glī’kə-jə-nŏl’ĭ-sĭs) n. Excessive glycogenolysis.

  • Hyperglycinuria

    hyperglycinuria hy·per·gly·ci·nu·ri·a (hī’pər-glī’sə-nur’ē-ə, -nyur’-) n. An abnormally high level of glycine in the urine.

  • Hyperglycorrhachia

    hyperglycorrhachia hy·per·gly·cor·rha·chi·a (hī’pər-glī’kə-rā’kē-ə, -rāk’ē-ə) n. The presence of excessive amounts of sugar in the cerebrospinal fluid.

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