Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 gene

Acta Neurol Belg. 2015 Dec;115(4):779-82. doi: 10.1007/s13760-014-0413-9. Epub 2014 Dec 28.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / physiopathology*
  • Bone Diseases, Developmental / genetics*
  • Bone Diseases, Developmental / physiopathology*
  • Brain Waves / genetics
  • Child
  • Electroencephalography
  • Facies
  • Humans
  • Intellectual Disability / genetics*
  • Intellectual Disability / physiopathology*
  • Male
  • Mutation / genetics*
  • Repressor Proteins / genetics*
  • Tooth Abnormalities / genetics*
  • Tooth Abnormalities / physiopathology*

Substances

  • ANKRD11 protein, human
  • Repressor Proteins

Supplementary concepts

  • KBG syndrome