| PKU | Phenyl-Keton-Uria; 페닐케톤뇨증 |
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| PKU | phenylketonuria |
| AR | 1) Aortic Regurgitation = AI Echo소견 &... |
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| PKU | Phenylketonuria |
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| 영문 | phenylketonuria(=PKU) | 한글 | 페닐케톤뇨증 |
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| 설명 | 선천병으로 체내에 페닐케톤이 축적되어 오줌으로 나오는 병이다. 폐닐케톤이 축적되는 이유는 인체내에 페닐알라닌(phenylalanine)이라는 아미노산을 다른 아미노산인 티로신으로 바꾸어 주는 한 효소(phenylalanine hydroxylase)가 선천적으로 결핍되어 태어나기 때문이다. 이 효소의 결핍이 있으면, 계속적인 페닐알라닌의 축적이 일어나고, 결국은 페닐케톤의 축적으로 발전한다. 신체내의 높은 페닐케톤농도는 태아의 뇌발달을 억제하여 결국은 정신지체를 유발한다. 따라서 이 질병은 빠른 진단으로, 페닐알라닌이 적은 식사(저단백질 식사)를 뇌의 발달이 완전히 멈추는 성인까지 시행하면, 자연히 치료된다. 신생아에서 이 질병의 존재를 알기 위해 오줌이나 혈액내에서, 페닐케톤의 유무를 알아보기도 하며, 구뜨리 진단법(Guthrie's test)을 시행한다. |
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| PKU | <disease> Congenital absence of phenylalanine hydroxylase (an enzyme that converts phenylalanine into tyrosine). Phenylalanine accumulates in blood and seriously impairs early neuronal development. The defect can be controlled by diet and is not serious if treated in this way. Incidence: highest in Caucasians. Acronym: PKU Origin: Gr. Ouron = urine (15 Oct 1997) |
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| non-PKU hyperphenylalaninaemia | A benign phenotype in which phenylalanine monooxygenase is deficient but is greater than 1% of normal levels. (05 Mar 2000) |
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| 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
출처: wordnet.princeton.edu/perl/webwn
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| 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.
출처: https://www.healthforums.com/library/1,1277,articl...
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| 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.
출처: helios.bto.ed.ac.uk/bto/glossary/p.htm
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| PKU |
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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| 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.
출처: www.nutrabio.com/Definitions/definitions_p.htm
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| PKU | a genetic disorder of metabolism |
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| PKU | a test of newborn infants for phenylketonuria |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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