Pseudo inherited left heart obstructive defects revealing a maternal phenylketonuria;Forme pseudo-hereditaire d'anomalies obstructives du coeur gauche revelatrice de phenylcetonurie maternelle

Archives des Maladies du Coeur et des Vaisseaux

Volumn 93, Issue 5, 2000, Pages 649-652

  Saliba, Z ^a   Bah, G ^a   Martin, D ^a   Abadie, V ^a   Azar, Z ^a   Fraisse, A ^a   Sidi, D ^a   Kachaner, J ^a   Bonnet, D ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE;

ARTICLE; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; DIAGNOSTIC PROCEDURE; FAMILY STUDY; HUMAN; INTRAUTERINE GROWTH RETARDATION; MATERNAL NUTRITION; MICROCEPHALY; PHENYLKETONURIA; BLOOD; CASE REPORT; FEMALE; GENETICS; MALE; NEWBORN; NUCLEAR FAMILY; PEDIGREE; PREGNANCY; PREGNANCY COMPLICATION;

FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; INFANT, NEWBORN; MALE; MICROCEPHALY; NUCLEAR FAMILY; PEDIGREE; PHENYLALANINE; PHENYLKETONURIAS; PREGNANCY; PREGNANCY COMPLICATIONS;

EID: 0034184519     PISSN: 00039683     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. Rouse B, Azen C, Koch R et al. Maternal Phenylketonuria Collaborative Study (MPKUCS) offsprings: facial anomalies, malformations, and early neurological sequealae. Am J Med Genet 1997 ; 69 : 89-95.
2. Koch R, Levy H, Hanley W et al. Outcome implications of the International Maternal Phenylketonuria Collaborative Study (MPKUCS): 1994. Eur J Pediatr 1996 ; 155 (suppl. 1) : S162-S164.
3. McDonald JD, Dyer CA, Gailis L, Kirby ML. Cardiovascular defects among the progeny of mouse phenylketonuria females. Pediatr Res 1997 ; 42 : 103-7.
4. Brenton DP. Cardiac defects in the children of mothers with high concentrations of plasma phenylalanine. Br Heart J 1990 ; 63 : 143-4.
5. Levy HL, Ghavami M. Maternal phenylketonuria: a metabolic teratogen. Teratology 1996 ; 53 : 176-84.
6. Kirby M, Miyagawa S. The effect of high phenylalanine concentration on chick embryonnic development. J Inherit Metab Dis 1990 ; 13 : 634-40.
7. Okano Y, Chow IZ, Isshiki G, Inoue A, Oura T. Effects of pnenylalanine loading on protein synthesis in the fetal heart and brain of rat: an experimental approach to maternal phenylketonuria. J Inherit Metab Dis 1986 ; 9 : 15-24.
8. Henglein D, Niederhoff H, Bode H. Origin of the left coronary artery from the right pulmonary artery and ventricular septal defect in a chid of a mother with rised plasma phenylalanine concentrations throughout pregnancy. Br Heart J 1990 ; 63 : 180-5.
9. Heifetz SA, Robinowitz M, Mueller KH, Virmani R. Total anomalous origin of the coronary arteries from the pulmonary artery. Pediatr Cardiol 1986 ; 7 : 11-8.
10. Franco B, Meroni G, Parenti G et al. A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) aand implications for warfarin embryopathy. Cell 1995 ; 81 : 15-25.