6p21.33 Deletion encompassing CSNK2B is associated with relative macrocephaly, facial dysmorphism, and mild intellectual disability

Clin Dysmorphol. 2021 Jul 1;30(3):139-141. doi: 10.1097/MCD.0000000000000372.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics
  • Casein Kinase II / genetics*
  • Casein Kinase II / metabolism
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 6 / genetics*
  • Craniofacial Abnormalities / genetics
  • Gene Deletion
  • Humans
  • Intellectual Disability / genetics
  • Male
  • Megalencephaly / genetics
  • Musculoskeletal Abnormalities / genetics
  • Phenotype
  • Syndrome

Substances

  • Casein Kinase II