Letter to the Editor
Prenatal genetic confirmation of a COL4A1 mutation presenting with sonographic fetal intracranial hemorrhage
Version of Record online: 9 MAY 2012
Copyright © 2012 ISUOG. Published by John Wiley & Sons, Ltd.
Ultrasound in Obstetrics & Gynecology
Volume 39, Issue 6, pages 726–727, June 2012
How to Cite
Lichtenbelt, K. D., Pistorius, L. R., De Tollenaer, S. M., Mancini, G. M. and De Vries, L. S. (2012), Prenatal genetic confirmation of a COL4A1 mutation presenting with sonographic fetal intracranial hemorrhage. Ultrasound Obstet Gynecol, 39: 726–727. doi: 10.1002/uog.11070
- Issue online: 28 MAY 2012
- Version of Record online: 9 MAY 2012
- Accepted manuscript online: 5 JAN 2012 11:30AM EST
|uog_11070_sm_suppinfotabs1.doc||40K||Supporting Information: Table S1. Summary of prenatal ultrasound and magnetic resonance imaging findings in cases with a COL4A1 mutation.|
|uog_11070_sm_suppinfofigs1.tif||2651K||Supporting Information: Figure S1. (a) Prenatal ultrasound image at 32 + 4 weeks' gestation showing cystic evolution of the chogenic lesion into a porencephalic cyst. (b) Postnatal magnetic resonance imaging (T2SE-weighted), axial views. The left cerebellar hemisphere is absent. There is an area of cavitation in the left basal ganglia. (c) Myelination is only seen as low signal intensity in the right posterior limb of the internal capsule.|
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