Late-onset hemophagocytic lymphohistiocytosis with neurological presentation

Sarah Benezech1, Thierry Walzer2, Emily Charrier2

  • 1Department of Pediatrics Hospices Civils de Lyon Lyon France.

Clinical Case Reports
|November 21, 2017
PubMed

Missense mutations in genes involved in familial hemophagocytic lymphohistiocytosis can delay the onset of this life-threatening disease. In children and adults, early recognition of aspecific features as neurological symptoms is crucial as urgent treatment is required.