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Condition

Autoimmune Lymphoproliferative Syndrome

General Healthcare

Overview

Rare congenital lymphoid disorder due to mutations in certain Fas-Fas ligand pathway genes. Known causes include mutations in FAS, TNFSF6, NRAS, CASP8, and CASP10 proteins. Clinical features include LYMPHADENOPATHY; SPLENOMEGALY; and AUTOIMMUNITY.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Autoimmune Lymphoproliferative Syndrome

Topic type
Condition
Category
General Healthcare
MeSH classification
C15.604.515.138|C16.320.089|C20.111.288|C20.683.515.124

Preparing for an appointment about Autoimmune Lymphoproliferative Syndrome

If you are speaking with a healthcare professional about Autoimmune Lymphoproliferative Syndrome, it can help to prepare a few details in advance.

  • Write down your symptoms and when they started.
  • Bring details of any medicines, supplements or previous treatments.
  • Ask what tests or assessments may be needed.
  • Ask what treatment or management options may be suitable.
  • Ask when you should seek urgent medical help or follow-up care.

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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.