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La phénylcétonurie (PCU) est une maladie héréditaire du métabolisme qui touche en France environ une naissance sur 15 000. Elle bénéficie d'un dépistage néonatal systématique, régionalisé et coordonné depuis 1978 grâce à l'action de l'Association française pour le dépistage et la prévention des handicaps de l'enfant (AFDPHE). Néanmoins, aucun consensus national sur la prise en charge des enfants dépistés...
Set the date range to filter the displayed results. You can set a starting date, ending date or both. You can enter the dates manually or choose them from the calendar.