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Late-onset hemophagocytic lymphohistiocytosis with neurological presentation.

Sarah BenezechThierry WalzerEmily CharrierDamien HeidelbergGeneviève De Saint-BasileYves BertrandAlexandre Belot
Published in: Clinical case reports (2017)
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.
Keyphrases
  • late onset
  • early onset
  • young adults
  • intellectual disability
  • cerebral ischemia
  • depressive symptoms
  • physical activity
  • smoking cessation