MATERNAL PHENYLKETONURIA PREGNANCY OUTCOME - A PRELIMINARY-REPORT OF FACIAL DYSMORPHOLOGY AND MAJOR MALFORMATIONS

被引:35
作者
ROUSE, B
LOCKHART, L
MATALON, R
AZEN, C
KOCH, R
HANLEY, W
LEVY, H
DELACRUZ, F
FRIEDMAN, E
机构
[1] UNIV ILLINOIS,CHICAGO,IL 60680
[2] CHILDRENS HOSP LOS ANGELES,LOS ANGELES,CA
[3] TORONTO CHILDRENS HOSP,TORONTO,ONTARIO,CANADA
[4] MASSACHUSETTS GEN HOSP,BOSTON,MA 02114
关键词
D O I
10.1007/BF01799376
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It is clear from the preliminary data that major malformations, i.e. intrauterine growth retardation, microcephaly and cardiac defects, tend to decrease in frequency as the blood phenylalanine level drops, but not enough to suggest that phenylalanine levels of 600 μmol/L are safe levels. The facial dysmorphic features may be used as a sensitive indicator that blood phenylalanine levels should be below 360 μmol/L. It is hoped that at the end of the collaborative study more data will be available to suggest blood phenylalanine levels which will prevent the deleterious effects of maternal PKU syndrome. © 1990 SSIEM and Kluwer Academic Publishers.
引用
收藏
页码:289 / 291
页数:3
相关论文
共 3 条
[1]  
DENT CE, 1957, 23RD ROSS PED RES C, P32
[2]   MATERNAL PHENYLKETONURIA AND HYPERPHENYLALANINEMIA - AN INTERNATIONAL SURVEY OF THE OUTCOME OF UNTREATED AND TREATED PREGNANCIES [J].
LENKE, RR ;
LEVY, HL .
NEW ENGLAND JOURNAL OF MEDICINE, 1980, 303 (21) :1202-1208
[3]   MATERNAL PHENYLKETONURIA - A CAUSE OF MENTAL RETARDATION IN CHILDREN WITHOUT METABOLIC DEFEC [J].
MABRY, CC ;
NELSON, TL ;
SON, CD ;
DENNISTON, JC .
NEW ENGLAND JOURNAL OF MEDICINE, 1963, 269 (26) :1404-+