Bilateral frontoparietal polymicrogyria (BFPP) syndrome secondary to a 16q12.1-q21 chromosome deletion involving GPR56 gene

Clin Genet. 2009 Dec;76(6):573-6. doi: 10.1111/j.1399-0004.2009.01262.x. Epub 2009 Oct 6.
No abstract available

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 16 / genetics*
  • Comparative Genomic Hybridization
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Magnetic Resonance Imaging
  • Male
  • Malformations of Cortical Development / complications*
  • Malformations of Cortical Development / genetics*
  • Pregnancy
  • Receptors, G-Protein-Coupled / genetics*
  • Syndrome

Substances

  • ADGRG1 protein, human
  • Receptors, G-Protein-Coupled