Brachmann-de Lange syndrome is characterized by pre- and postnatal growth r
etardation, microbrachycephaly, hirsutism, various visceral and limb anomal
ies and a typical face. A sonographic prenatal diagnosis at mid-trimester i
s reported in a case of severe, symmetrical fetal growth delay at 20 weeks
gestation, with a thickened skin on the forehead, a small nose and a marked
depressed nasal bridge, a long philtrum, micrognathia and a persistently f
lexed right forearm, with a single bone associated to oligodactyly. Due to
the severe mental impairment with a commonly estimated intelligence quotien
t under 60, the pregnancy was terminated after parental consent. (C) 1999 E
lsevier Science Ireland Ltd. All rights reserved.