Literature DB >> 8362914

Brain magnetic resonance imaging findings in the Opitz G/BBB syndrome: extension of the spectrum of midline brain anomalies.

M R MacDonald1, G B Schaefer, A H Olney, M Tamayo, J L Frías.   

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.

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Year:  1993        PMID: 8362914     DOI: 10.1002/ajmg.1320460622

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

Review 1.  Initial immunopathogenesis of multiple sclerosis: innate immune response.

Authors:  Norma Y Hernández-Pedro; Guillermo Espinosa-Ramirez; Verónica Pérez de la Cruz; Benjamín Pineda; Julio Sotelo
Journal:  Clin Dev Immunol       Date:  2013-09-24

2.  Mid1/Mid2 expression in craniofacial development and a literature review of X-linked opitz syndrome.

Authors:  Bijun Li; Tianhong Zhou; Yi Zou
Journal:  Mol Genet Genomic Med       Date:  2015-12-12       Impact factor: 2.183

3.  A surgical approach to the craniofacial defects of Opitz G/BBB syndrome.

Authors:  John P Regan; Karen Szymanski; Silvio Podda; Francesco Gargano; Anthony Kopiecki
Journal:  J Surg Case Rep       Date:  2017-02-17
  3 in total

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