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Nous rapportons un cas rare de discordance fœto-placentaire complète concernant un enfant porteur d’une trisomie 21. Une ponction de villosités choriales a été réalisée en raison d’une hyperclarté nucale. Le caryotype obtenu était 46,XX sur l’examen direct et la culture cellulaire. En raison d’une dysmorphie faciale associée à une cardiopathie chez l’enfant, un caryotype sanguin a été proposé. Ce...
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