| phenylketonuria |
a genetic disorder of metabolism; lack of the enzyme needed to turn phenylalanine into tyrosine results in an accumulation of phenylalanine in the body fluids which causes various degrees of mental deficiency
출처: wordnet.princeton.edu/perl/webwn
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| phenylketonuria |
a hereditary disorder in which the enzyme that converts the amino acid phenylalanine into another amino acid is defective, meaning phenylalanine must be kept out of the diet
출처: www.american-depot.com/services/resources_gl_p.asp
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| phenylketonuria |
a disease that prevents the body from processing a specific part of protein called phenylalanine. The buildup of this substance in the body leads to mental retardation if the child does not have a special diet from birth.
출처: https://www.healthforums.com/library/1,1277,articl...
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| phenylketonuria |
A congenital condition in which the body lacks a specific enzyme. This causes abnormal metabolism that may result in brain damage.
출처: www.cnn.com/HEALTH/library/BN/00023.html
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| phenylketonuria |
An inherited disorder resulting in the inability to process the amino acid, phenylananine. If not treated, the disorder may result in mental retardation. Treatment is a diet low in phenylalanine. Newborns are screened for PKU, in order to determine the need for treatment before brain damage occurs.
출처: www.nutrabio.com/Definitions/definitions_p.htm
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