hrp0082p2-d1-564 | Sex Development | ESPE2014
Baetens Dorien
, Mladenov Wilhelm
, Chiaie Barbara Delle
, Desloovere An
, Iotova Violeta
, Menten Bjorn
, Van Laecke Eric
, Hoebeke Piet
, De Baere Elfride
, Cools Martine
Background: Extensive and time-consuming hormonal and genetic work-up provides a genetic diagnosis in around 20% of 46,XY cases with ambiguous genitalia. It is currently unclear if such extensive screening might also be indicated in 46,XY newborns with milder undervirilization.Method: All 46,XY neonates and infants (n=32, EMS 212) referred to our pediatric endocrine service for atypical male genitalia in the period 20072013 were inve...