Shift of the fetal sex ratio in hCG selected pregnancies at risk for Down syndrome

1992 ◽  
Vol 12 (8) ◽  
pp. 703-704 ◽  
Author(s):  
Nathalie Leporrier ◽  
Michel Herrou ◽  
Pierre Leymarie
Keyword(s):  
At Risk ◽  
1979 ◽  
Vol 31 (3) ◽  
pp. 246-250 ◽  
Author(s):  
R.F. DiGiacomo ◽  
P.W. Shaughnessy
Keyword(s):  

Diabetes ◽  
2001 ◽  
Vol 50 (5) ◽  
pp. 1193-1199 ◽  
Author(s):  
A. F. Machado ◽  
E. F. Zimmerman ◽  
D. N. Hovland ◽  
R. Weiss ◽  
M. D. Collins

1997 ◽  
Vol 75 (4) ◽  
pp. 648-650 ◽  
Author(s):  
Eigil Reimers ◽  
Dag Lenvik

Theory suggests that a male in good condition at the end of the period of parental investment will outproduce a sister in similar condition, while she will outproduce him if both are in poor condition. Accordingly, natural selection should favor parental ability to adjust the sex ratio of offspring produced according to parental ability to invest. As maternal condition declines from good to poor, the fetal sex ratio should decline from a high proportion of males to a high proportion of females. Data from 1525 domestic reindeer (Rangifer tarandus) in six different herds slaughtered during December and January in 1976 through 1979 do not support a relationship between the sex of the fetus and either the condition of the mother or her age.


Blood ◽  
2013 ◽  
Vol 122 (24) ◽  
pp. 3908-3917 ◽  
Author(s):  
Irene Roberts ◽  
Kate Alford ◽  
Georgina Hall ◽  
Gaetan Juban ◽  
Helen Richmond ◽  
...  

Key Points GATA1 mutations are common in neonates with Down syndrome but are often unsuspected and detectable only with sensitive methods. Multilineage blood abnormalities in all Down syndrome neonates in the absence of GATA1 mutations suggests that trisomy 21 itself perturbs hemopoiesis.


Children ◽  
2020 ◽  
Vol 7 (6) ◽  
pp. 52
Author(s):  
Zachary Prudowsky ◽  
HyoJeong Han ◽  
Alexandra Stevens

Transient abnormal myelopoiesis (TAM) is a common and potentially fatal neonatal complication of newborn babies with Down syndrome (DS). Children born with mosaic DS are also at risk of developing TAM. However, due to their variable phenotypes, early identification of patients with mosaic DS may be difficult; thus, early diagnosis of TAM is just as challenging. In this report, we describe a case of a phenotypically normal newborn who presented with concerns for neonatal leukemia. The diagnosis of mosaic DS and TAM was confirmed with abnormal GATA1 mutation testing, highlighting the importance of early GATA1 mutation testing in newborn leukemia with high suspicion for TAM.


2006 ◽  
Vol 195 (6) ◽  
pp. S193
Author(s):  
Patrizia Vergani ◽  
Alessandro Ghidini ◽  
Steven Weiner ◽  
Anna Biffi ◽  
Anna Locatelli ◽  
...  

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