Neurological Abnormality Could be the First and Only Symptom of Familial Hemophagocytic Lymphohistiocytosis: Report of Two Families

Chin Med J (Engl). 2018 Dec 20;131(24):3004-3006. doi: 10.4103/0366-6999.247206.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Central Nervous System Diseases / etiology*
  • Child
  • Female
  • Humans
  • Infant
  • Lymphohistiocytosis, Hemophagocytic / complications
  • Lymphohistiocytosis, Hemophagocytic / diagnosis*
  • Lymphohistiocytosis, Hemophagocytic / genetics
  • Magnetic Resonance Imaging
  • Male
  • Mutation
  • Perforin / genetics

Substances

  • PRF1 protein, human
  • Perforin