Hypereosinophilic syndrome and hemimelia in a patient with chromosome 6p22.3 deletion

Pediatr Allergy Immunol. 2014 Aug;25(5):500-3. doi: 10.1111/pai.12213. Epub 2014 Mar 16.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 6 / genetics*
  • Ectromelia / genetics*
  • Humans
  • Hypereosinophilic Syndrome / genetics*
  • Infant
  • Infant, Newborn
  • Male