See Also: citrullinaemia(medicine)
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citrullinaemia (medicine)


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.