Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2-p13.12/13 deletion

Am J Hematol. 2017 Jan;92(1):E2-E3. doi: 10.1002/ajh.24574. Epub 2016 Nov 12.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Chromosome Deletion*
  • Chromosomes, Human, Pair 19 / genetics*
  • Craniosynostoses* / blood
  • Craniosynostoses* / genetics
  • Female
  • Fetal Hemoglobin / genetics
  • Fetal Hemoglobin / metabolism*
  • Humans
  • Kruppel-Like Transcription Factors / genetics*
  • Language Development Disorders* / blood
  • Language Development Disorders* / genetics
  • Male
  • Psychomotor Disorders* / blood
  • Psychomotor Disorders* / genetics

Substances

  • Kruppel-Like Transcription Factors
  • erythroid Kruppel-like factor
  • Fetal Hemoglobin