Maternal phenylketonuria

Obstetrics and Gynecology

Volumn 114, Issue 6, 2009, Pages 1432-1433

[No Author Info available]

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE; PHENYLALANINE 4 MONOOXYGENASE; TYROSINE;

AUTOSOMAL RECESSIVE INHERITANCE; DIET THERAPY; EMBRYOPATHY; FAMILY PLANNING; FEMALE; GENE MUTATION; GENETIC COUNSELING; HUMAN; HYPERPHENYLALANINEMIA; MATERNAL CARE; NOTE; PHENYLKETONURIA; PRIORITY JOURNAL; PROTEIN METABOLISM; PROTEIN RESTRICTION; ARTICLE; FETUS DISEASE; PREGNANCY;

FAMILY PLANNING SERVICES; FEMALE; FETAL DISEASES; GENETIC COUNSELING; HUMANS; PHENYLKETONURIA, MATERNAL; PREGNANCY;

EID: 73449095429     PISSN: 00297844     EISSN: None     Source Type: Journal    
DOI: 10.1097/AOG.0b013e3181c6f93d     Document Type: Note

References (5)

1. Lenke RR, Levy HL. Maternal phenylketonuria and hyper-phenylalaninemia. An international survey of the outcome of untreated and treated pregnancies. N Engl J Med 1980; 303:1202-1208
2. Widaman KF, Azen C. Relation of prenatal phenylalanine exposure to infant and childhood cognitive outcomes: results from the International Maternal PKU Collaborative Study. Pediatrics 2003;112:1537-1543
3. Matalon KM, Acosta PB, Azen C. Role of nutrition in pregnancy with phenylketonuria and birth defects. Pediatrics 2003;112:1534-1536
4. Brown AS, Fernhoff PM, Waisbren SE, Frazier DM, Singh R, Rohr F, et al. Barriers to successful dietary control among pregnant women with phenylketonuria. Genet Med 2002; 4:84-89
5. Levy HL, Waisbren SE, Lobbregt D, Allred E, Schuler A, Trefz FK, et al. Maternal mild hyperphenylalaninaemia: an international survey of offspring outcome. Lancet 1994; 344:1589-1594