Trizygotic dichorionic triplets with 46,XX/46,XY chimerism in both fetuses of the monochorionic pair.
نویسندگان
چکیده
Monochorionic fetuses are traditionally thought of as monozygotic (MZ), arising from a single embryo that splits during early embryogenesis. With rare exception, they typically exhibit the same genotype and the same gender. However, several recent reports have documented that monochorionicity does not always indicate monozygosity (Souter et al., 2003). At least 14 such cases have been reported (Ekelund et al., 2008). We report a trizygotic triplet pregnancy conceived by in vitro fertilization (IVF) in which triamniotic dichorionic placentation was identified in addition to hematopoietic chimerism in the monochorionic pair. A 29-year-old Caucasian, insulin-dependent diabetic woman gravida 2, para 1, conceived a triplet gestation with the assistance of IVF. Three embryos were transferred. An ultrasound performed at 7 weeks revealed three viable embryos in three gestational sacs. A thin membrane, with a direct, perpendicular insertion into a single placenta, was visualized between sacs B and C. There was no evidence of a lambda sign at the placental insertion site. These findings indicated monochorionicity between the B and C sacs. Fetus A was surrounded by a single amnion and a single chorion. The sonographic findings indicated a triamniotic, dichorionic triplet pregnancy. Genotypes of the B and C embryos were assumed to be identical due to the observed monochorionicity. At 12 weeks and 5 days, the ultrasound findings were confirmed. As part of a Down syndrome risk assessment, nuchal translucency measurements were 1.9, 1.3 and 2.2 mm, for triplets A, B and C, respectively. Ultrasound at 18 weeks revealed a gender discrepancy between the monochorionic fetuses, with triplet B demonstrating normal appearing female external genitalia and triplet C demonstrating normal appearing male external genitalia. Fetus A was noted to be female. Due to the gender discrepancy, amniocentesis was performed on all three gestational sacs. Separate needle insertions were performed for each fetus. Following withdrawal
منابع مشابه
Blood chimerism in a dizygotic dichorionic pregnancy.
Blood chimerism in twins is known to occur through the transfer of hematopoietic stem cells between the fetuses via a common placenta. We present a case of blood chimerism in a dizygotic dichorionic twin pregnancy. The female twin was delivered at 34 weeks of gestation, and the male twin was stillborn. Pathologic examination confirmed dichorionic diamniotic placentas. The karyotype of the femal...
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Prenatal diagnosis of simultaneous occurrence of chimerism and autosomal mosaicism is extremely rare. We report the prenatal diagnosis and genetic analysis of a fetus in a twin pregnancy with mosaic 47,XX,+21/46,XX with chimeric XX/XY. A 36-year-old, para 1, woman was referred for genetic counseling at 20 weeks' gestation because of abnormal karyotype (47,XX,+21/46,XX) in one fetus in a twin pr...
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Chimerism is rare in humans and is usually discovered accidentally when a 46,XX and 46,XY karyotype is found in a same individual. We describe a malformed female infant with neural tube defect (NTD) and a 47,XY,+21[5]/46,XX[30] karyotype.
متن کاملIntrauterine growth in multiple pregnancies in relation to fetal number, chorionicity and gestational age.
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متن کاملNuchal translucency in multiple pregnancies.
AIM To evaluate the prevalence of increased nuchal translucency (NT) in multiple pregnancies and its relation to fetal karyotype and pregnancy outcome. METHODS We measured fetal nuchal translucency (NT) in 6,338 women pregnant from 10+3 to 13+6 weeks by ultrasound and evaluated the prevalence of NT=95th centile in 115 multiple pregnancies, including 100 pairs of twins (70 dichorionic and 30 m...
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ورودعنوان ژورنال:
- Prenatal diagnosis
دوره 29 11 شماره
صفحات -
تاریخ انتشار 2009