A patient with chromosome 18p deletion and congenital hypoglossia

Clin Dysmorphol. 2018 Apr;27(2):46-48. doi: 10.1097/MCD.0000000000000207.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosome Disorders / genetics*
  • Chromosome Disorders / physiopathology
  • Chromosomes, Human, Pair 18 / genetics
  • Female
  • Holoprosencephaly / genetics*
  • Holoprosencephaly / physiopathology
  • Humans
  • Infant, Newborn
  • Karyotyping
  • Stomatognathic System Abnormalities / genetics*
  • Stomatognathic System Abnormalities / physiopathology