Condition

Autoimmune lymphoproliferative syndrome

Diseases of the Blood and Immune Mechanism

Autoimmune lymphoproliferative syndrome, often shortened to ALPS, is a rare genetic form of lymphoproliferative disorder in which lymphocytes survive abnormally because Fas mediated apoptosis is defective. Normally the immune system down-regulates after an infection as Fas and Fas ligand trigger the death of activated B and T cells; in ALPS this pathway fails, leading to chronic non-malignant lymphoproliferation, autoimmune disease and an increased risk of cancers such as Hodgkin and non-Hodgkin lymphoma. Typical signs are enlarged lymph nodes and spleen, and the most common autoimmune problems are hemolytic anemia, neutropenia and thrombocytopenia. The condition is usually caused by mutations in the FAS gene and is inherited in an autosomal dominant manner with incomplete penetrance, so that up to 40 percent of people with a FAS mutation show no symptoms. Diagnosis rests on chronic non-malignant lymphoproliferation, elevated double-negative T cells and supporting laboratory criteria.

Facts
Classification
Body System
Lymphatic or Immune System 1
ICD-10 Chapter
III: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism 2
Communicable or Non-communicable
Non-Communicable 1
Transmission Route
Non-Transmissible 1
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
Sources
1. MedlinePlus: Autoimmune Lymphoproliferative Syndrome - MedlinePlus Genetics
MedlinePlus
  • Description
    Autoimmune lymphoproliferative syndrome (ALPS) is an inherited disorder in which the body cannot properly regulate the number of immune system cells (lymphocytes).
  • Causes
    Mutations in the FAS gene cause ALPS in approximately 75 percent of affected individuals
  • Inheritance
    this condition is inherited in an autosomal dominant pattern, which means one copy of an altered gene in each cell is sufficient to cause the disorder.
  • Inheritance, inherited from a parent
    an affected person usually inherits the mutation from one affected parent.
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2. EMBL-EBI Ontology Lookup Service: autoimmune lymphoproliferative syndrome (MONDO term)
EMBL-EBI Ontology Lookup Servicedatabase_cross_reference of the MONDO term autoimmune lymphoproliferative syndrome; ICD-10 chapter derived from code D89.82 (WHO range D50-D89)
Quote, database_cross_reference of the MONDO term autoimmune lymphoproliferative syndrome; ICD-10 chapter derived from code D89.82 (WHO range D50-D89)
ICD10CM:D89.82
View the Source
Autoimmune lymphoproliferative syndrome (Wikipedia)
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