Periventricular heterotopia with white matter abnormalities associated with 6p25 deletion

Am J Med Genet A. 2012 Jul;158A(7):1793-7. doi: 10.1002/ajmg.a.35416. Epub 2012 Jun 7.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Child
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 6*
  • Comparative Genomic Hybridization
  • Female
  • Forkhead Transcription Factors / genetics
  • Humans
  • Leukoencephalopathies / complications
  • Leukoencephalopathies / diagnosis
  • Leukoencephalopathies / genetics*
  • Magnetic Resonance Imaging
  • Male
  • Neuroimaging
  • Periventricular Nodular Heterotopia / complications
  • Periventricular Nodular Heterotopia / diagnosis
  • Periventricular Nodular Heterotopia / genetics*

Substances

  • FOXC1 protein, human
  • Forkhead Transcription Factors

Supplementary concepts

  • Periventricular Laminar Heterotopia