📣Thông báo: Một trường hợp “rất” hiếm gặp - Hội chứng FG type 1 (FG syndrome type 1) do đột biến gen MED12 (gen trội liên kết NST X) gây bất thường não, tim, và nhiều cơ quan khác😰 Thai phụ 34 tuổi, đã có 1 cô con gái năm nay 4 tuổi khoẻ mạnh bình thường, lần mang thai này là lần thứ 2 (giống bố). Cách đây hơn 1 tháng, tại thời điểm thai được 23w thai phụ được sự giới thiệu của bạn bè, người thân - tìm đến chỗ chúng tôi siêu âm lần đầu với chẩn đoán của tuyến trước là “giãn nhẹ não thất bên”.
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📣Thông báo: Một trường hợp “rất” hiếm gặp - Hội chứng FG type 1 (F…
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