Lobar holoprosencephaly: Prenatal MR diagnosis with postnatal MR correlation

Alex M.C. Wong, Larissa T. Bilaniuk, K. K. Ng, Y. L. Chang, A. S. Chao*, Y. Y. Wai

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

14 Scopus citations

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.

Original languageEnglish
Pages (from-to)296-299
Number of pages4
JournalPrenatal Diagnosis
Volume25
Issue number4
DOIs
StatePublished - 04 2005
Externally publishedYes

Keywords

  • Lobar holoprosencephaly
  • MRI
  • Prenatal diagnosis

Fingerprint

Dive into the research topics of 'Lobar holoprosencephaly: Prenatal MR diagnosis with postnatal MR correlation'. Together they form a unique fingerprint.

Cite this