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- W1513635447 startingPage "53" @default.
- W1513635447 abstract "XYY sendromu 47, XYY karyotipi ile birlikte gorulen nadir bir cinsiyet kromozomu bozuklugudur. Kromozomal ayrilmadaki bir defektten kaynaklanir. Prenatal tanisi zordur cunku bu tabloda sonografik olarak saptanabilen anomalilerle birliktelik yoktur. 23 yasindaki bir gebe kadin klinigimize basvurdu. 18. gebelik haftasinda yapilan uclu tarama testinde trizomi 21 riski 1/56 olarak hesaplandi. 21. gebelik haftasinda yapilan ultrasonografide ventrikulomegali saptandi. Bu nedenle, amniyosentez yapildi ve fetusun anormal 47, XYY karyotipine sahip oldugu bulundu. Bu vaka sunumu ile 47 XYY sendromunun tani ve tedavisindeki son ilerlemeleri gozden gecirmeyi amacladik." @default.
- W1513635447 created "2016-06-24" @default.
- W1513635447 creator A5024687379 @default.
- W1513635447 date "2012-03-01" @default.
- W1513635447 modified "2023-09-24" @default.
- W1513635447 title "PRENATAL 47 XYY SENDROMU VE VENTRİKÜLOMEGALİ BİRLİKTELİĞİ: VAKA SUNUMU" @default.
- W1513635447 doi "https://doi.org/10.16919/btd.24394" @default.
- W1513635447 hasPublicationYear "2012" @default.
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