TY - ABST
T1 - Abnormal fetal head shape
T2 - Diagnosis and management
AU - Petersen, O. B.
AU - Gardener, G.J.
AU - Chitty, Lyn S
PY - 2003/1/1
Y1 - 2003/1/1
N2 - An abnormal head shape is an uncommon finding on prenatal ultrasound, associated most commonly with spina bifida, aneuploidy or oligohydramnios. In other cases diagnosis can be difficult. The objective of this study was to define management pathways for the investigation of fetuses with an abnormal head shape. Fetuses with an abnormal skull shape seen over a 10-year period in our unit were identified by searching the computerised database. Sonographic findings, diagnosis and outcome were reviewed. Three hundred and thirty-one cases were identified, the majority being associated with spina bifida (30%, lemon-shaped), aneuploidy (12%, strawberry-shaped) or dolicocephaly (18%) secondary to fetal position or oligohydramnios. Of the remainder, eight had craniosynostosis, three of which had a skeletal dysplasia. There was also one fetus each with Aperts syndrome, Saethre Chotzen syndrome and I-cell disease and two with an as yet undefined craniosynostosis sydrome.
AB - An abnormal head shape is an uncommon finding on prenatal ultrasound, associated most commonly with spina bifida, aneuploidy or oligohydramnios. In other cases diagnosis can be difficult. The objective of this study was to define management pathways for the investigation of fetuses with an abnormal head shape. Fetuses with an abnormal skull shape seen over a 10-year period in our unit were identified by searching the computerised database. Sonographic findings, diagnosis and outcome were reviewed. Three hundred and thirty-one cases were identified, the majority being associated with spina bifida (30%, lemon-shaped), aneuploidy (12%, strawberry-shaped) or dolicocephaly (18%) secondary to fetal position or oligohydramnios. Of the remainder, eight had craniosynostosis, three of which had a skeletal dysplasia. There was also one fetus each with Aperts syndrome, Saethre Chotzen syndrome and I-cell disease and two with an as yet undefined craniosynostosis sydrome.
UR - http://www.scopus.com/inward/record.url?scp=85018935368&partnerID=8YFLogxK
U2 - 10.1080/718591728
DO - 10.1080/718591728
M3 - Conference abstract in journal
AN - SCOPUS:85018935368
VL - 23
SP - S39-S39
JO - Journal of Obstetrics and Gynaecology
JF - Journal of Obstetrics and Gynaecology
SN - 0144-3615
IS - sup1
ER -