| MHPA | mild hyperphenylalaninemia |
|---|
| HPA | Hyperphenylalaninemia |
|---|
| hyperphenylalaninemia |
1. any of several autosomal recessive defects in the hydroxylation of phenylalanine resulting in accumulation and excretion of dietary phenylalanine. Most commonly the defect is in the enzyme phenylalanine 4-monooxygenase; the most severe manifestation of this is classic phenylketonuria (q.v.), but two benign forms also occur (see transient h. and persistent h.). Rarely, the defect is one of tetrahydrobiopterin metabolism; see malignant h. 2. excess of phenylalanine in the blood.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|