¼±Åà - È­»ìǥŰ/¿£ÅÍŰ ´Ý±â - ESC

 
"PKU"¿¡ ´ëÇÑ ¼¼ºÎ °Ë»ö °á°úÀÔ´Ï´Ù
KMLE À¥ ¿ë¾î ¸ÂÃã °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
PKU 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
Ãâó: wordnet.princeton.edu/perl/webwn
PKU 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.
Ãâó: https://www.healthforums.com/library/1,1277,articl...
PKU A human metabolic disease caused by a mutation in a gene coding for a phenylalanine processing enzyme (phenylalanine hydroxylase), which leads to accumulation of phenylalanine and mental retardation if not treated; inherited as an autosomal recessive phenotype.
Ãâó: helios.bto.ed.ac.uk/bto/glossary/p.htm
PKU A congenital condition in which the body lacks a specific enzyme. This causes abnormal metabolism that may result in brain damage.
Ãâó: www.cnn.com/HEALTH/library/BN/00023.html
PKU 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.
Ãâó: www.nutrabio.com/Definitions/definitions_p.htm
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
KMLE À¥ ¿ë¾î À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
ÅëÇÕ°Ë»ö ¿Ï·á