In utero and early postnatal presentation of autoimmune lymphoproliferative syndrome in a family with a novel FAS mutation

Haematologica. 2013 Apr;98(4):e38-9. doi: 10.3324/haematol.2012.070524. Epub 2012 Sep 14.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Autoimmune Lymphoproliferative Syndrome / diagnosis
  • Autoimmune Lymphoproliferative Syndrome / genetics*
  • DNA Mutational Analysis
  • Family Health
  • Female
  • Fetal Diseases / diagnosis
  • Fetal Diseases / genetics*
  • Humans
  • Infant, Newborn
  • Mutation*
  • Pregnancy
  • Prenatal Diagnosis
  • fas Receptor / genetics*

Substances

  • FAS protein, human
  • fas Receptor