| Literature DB >> 15849803 |
Alex M-C Wong1, Larissa T Bilaniuk, K-K Ng, Y-L Chang, A-S Chao, Y-Y Wai.
Abstract
Holoprosencephaly is a congenital anomaly characterized by lack of cleavage of the prosencephalon. Although, relatively rare, it is the most common anomaly that involves both the brain and the face. Prenatal diagnosis of this anomaly using ultrasonography, particularly of the less severe forms, is difficult. Magnetic resonance imaging has recently become an important complement to US in prenatal diagnosis of CNS anomalies. We herein report a patient in whom, at 23 weeks of gestation, US suggested agenesis of the corpus callosum and in whom, at 24 weeks of gestation, MRI correctly diagnosed lobar holoprosencephaly, which was confirmed by a postnatal MRI at 3 weeks of age.Entities:
Mesh:
Year: 2005 PMID: 15849803 DOI: 10.1002/pd.1108
Source DB: PubMed Journal: Prenat Diagn ISSN: 0197-3851 Impact factor: 3.050