Hypopigmented skin patches in 17q21.31 microdeletion syndrome: expanding the spectrum of cutaneous findings

Clin Dysmorphol. 2014 Jan;23(1):32-34. doi: 10.1097/MCD.0000000000000019.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / pathology
  • Adolescent
  • Chromosome Deletion
  • Chromosomes, Human, Pair 17 / genetics
  • Humans
  • Hypopigmentation / genetics*
  • Hypopigmentation / pathology
  • Infant, Newborn
  • Intellectual Disability / genetics*
  • Intellectual Disability / pathology
  • Karyotype
  • Male
  • Skin / pathology*

Supplementary concepts

  • Chromosome 17q21.31 Deletion Syndrome