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Le rétinoblastome est la tumeur intra-oculaire la plus fréquente de l’enfant. Le pronostic vital est excellent, et l’enjeu thérapeutique actuel est de préserver la fonction visuelle et de limiter les séquelles à moyen et long termes. Le risque de second cancer existe chez tout survivant d’un rétinoblastome, spécialement chez ceux porteurs d’une mutation du gène RB. Il est fortement augmenté par l’irradiation...
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.