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citrullinaemia A disease of amino acid metabolism (usually classed as a type of aminoaciduria) in which citrulline concentrations in blood, urine, and cerebrospinal fluid are elevated; manifested clinically by vomiting, ammonia intoxication, and mental retardation beginning in infancy; autosomal recessive inheritance.
(05 Mar 2000)
citrulline <chemical> Chemical name: L-Ornithine, N5-(aminocarbonyl)-
(12 Dec 1998)
citrullinuria Enhanced urinary excretion of citrulline; a manifestation of citrullinaemia.
(05 Mar 2000)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 2 ÆäÀÌÁö: 1
  • Citrulline - »õâ
    Synonyms :
  • Citrullinemia - »õâ A group of diseases related to a deficiency of the enzyme ARGININOSUCCINATE SYNTHASE which causes an elevation of serum levels of CITRULLINE. In neonates, clinical manifestations include lethargy, hypotonia, and SEIZURES. Milder forms also occur. Childhood and adult forms may present with recurrent episodes of intermittent weakness, lethargy, ATAXIA, behavioral changes, and DYSARTHRIA. (From Menkes, Textbook of Child Neurology, 5th ed, p49)
    Synonyms : Argininosuccinic Acid Synthase Deficiency Disease, Argininosuccinic Acid Synthetase Deficiency Disease, Argininosuccinic Acid Synthetase Deficiency Disease, Partial, Argininosuccinic Acid Synthetase Deficiency, Complete, Citrullinemia, Classical
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A01205091 Citrulline, N-acetyl-l-aspartic acid, Pyridoxine HCl, Retinol Acetate, Tocopherol Acetate, Vaccinium myrtillus extract
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Citrulline Malate
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Citrulline Malate
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citrulline an amino acid that does not occur in proteins but is an intermediate in the conversion of ornithine to arginine
Ãâó: wordnet.princeton.edu/perl/webwn
citrullinemia Citrullinemia is an inherited disorder that causes ammonia and other toxic substances to accumulate in the blood. Two forms of citrullinemia have been described; they have different signs and symptoms and are caused by mutations in different genes. Citrullinemia belongs to a class of genetic diseases called urea cycle disorders. The urea cycle is a sequence of chemical reactions that takes place in the liver. ...
Ãâó: en.wikipedia.org/wiki/Citrullinemia
citrullinuria 1. argininosuccinate synthase deficiency.  2. excretion of high levels of citrulline in the urine.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
WordNet ÀÏ¹Ý ¿µ¿µ »çÀü °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
citrullin an amino acid that does not occur in proteins but is an intermediate in the conversion of ornithine to arginine
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