Brain magnetic resonance imaging findings in the opitz G/BBB syndrome: Extension of the spectrum of midline brain anomalies

M. R. MacDonald, G. B. Schaefer, A. H. Olney, M. Tamayo, J. L. Frias

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17 Scopus citations

Abstract

We report the brain magnetic resonance imaging findings in 4 patients with the Opitz BBB/G syndrome. The scans were assessed by subjective interpretation and computerized image analysis. Findings noted in 3 of the 4 patients include hypoplasia or agenesis of the corpus callosum (3 patients), cerebellar vermal hypoplasia (2 patients), cortical atrophy and ventriculomegaly (3 patients), macro cisterna magna (3 patients), and a wide cavum septum pellucidum (1 patient). One patient had a normal scan. The demonstration of a wide cavum septum pellucidum extends the spectrum of midline brain anomalies (ventral induction defects) reported in this condition. This study along with other recent reports suggests that midline brain anomalies may be frequent findings in Opitz syndrome.

Original languageEnglish
Pages (from-to)706-711
Number of pages6
JournalAmerican Journal of Medical Genetics
Volume46
Issue number6
DOIs
StatePublished - 1993
Externally publishedYes

Keywords

  • cerebral dysgenesis
  • computerized image analysis
  • midline field defect

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