Phénylcétonurie maternelle [Maternal phenylketonuria]

Détails

ID Serval
serval:BIB_006B54CFB657
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Institution
Titre
Phénylcétonurie maternelle [Maternal phenylketonuria]
Périodique
Revue Médicale de la Suisse romande
Auteur⸱e⸱s
Matthieu J.M., Boulat O., Bianchi N.
ISSN
0035-3655
Statut éditorial
Publié
Date de publication
2001
Volume
121
Numéro
4
Pages
297-300
Langue
français
Notes
Publication types: Case Reports ; English Abstract ; Journal Article
Résumé
The child of a phenylketonuric woman is exposed during pregnancy to a high risk of growth retardation and malformation. The frequency of these abnormalities is proportional to the maternal phenylalanine blood concentrations. If a strict low protein diet is followed before conception and throughout gestation the risks of abnormalities are not higher than in the normal population. The maternal blood phenylalanine levels must be maintained between 120 and 250 mumol/l and the tyrosine blood levels between 45 and 90 mumol/l. Weekly blood analyses are mandatory. Regular dietary controls are necessary to assure that the adequate energetic intake and the correct amounts of vitamins and minerals recommended for a pregnant woman are sustained. A case report is the opportunity to discuss certain practical aspects concerning the monitoring of the pregnancy of a phenylketonuric woman and to make general recommendations.
Mots-clé
Adult, Congenital Abnormalities, Diet, Protein-Restricted, Energy Intake, Female, Fetal Growth Retardation, Gestational Age, Humans, Nutritional Requirements, Phenylalanine, Phenylketonuria, Maternal, Pregnancy, Prenatal Care, Risk Factors, Tyrosine
Pubmed
Création de la notice
05/02/2008 10:24
Dernière modification de la notice
20/08/2019 12:22
Données d'usage