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Autoimmune lymphoproliferative syndrome, type 1a(ALPS1A)

MedGen UID:
356453
Concept ID:
C1866119
Disease or Syndrome
Synonyms: ALPS1A; Autoimmune Lymphoproliferative Syndrome, Type Ia; AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IA, AUTOSOMAL RECESSIVE
 
OMIM®: 134637; 601859

Definition

A rare, primary immunodeficiency with an autosomal dominant pattern of inheritance but variable penetrance. It is the most common subtype of autoimmune lymphoproliferative syndrome (ALPS). It is usually caused by a germline mutation in the Fas gene that leads to defective Fas-induced apoptosis but in a minority of cases, it also may be attributed to a somatic Fas mutation. Disruption of Fas-induced apoptosis impairs lymphocyte homeostasis and immune tolerance. Characteristic laboratory findings include an increase in circulating, double-negative (CD4-/CD8-) T cells in the setting of immune-mediated anemia, thrombocytopenia and neutropenia. Clinical signs present in childhood include fatigue, pallor, bruising, hepatosplenomegaly and chronic, non-malignant, non-infectious lymphadenopathy. The clinical course is influenced by a strong association with other autoimmune disorders and an increased risk for developing Hodgkin and non-Hodgkin lymphoma. [from NCI]

Recent clinical studies

Etiology

Auricchio L, Vitiello L, Adriani M, Ferri P, Chiocchetti A, Pettinato G, Racioppi L, Maiuri L, Dianzani U, Pignata C
Dermatology 2005;210(4):336-40. doi: 10.1159/000084762. PMID: 15942224

Diagnosis

Auricchio L, Vitiello L, Adriani M, Ferri P, Chiocchetti A, Pettinato G, Racioppi L, Maiuri L, Dianzani U, Pignata C
Dermatology 2005;210(4):336-40. doi: 10.1159/000084762. PMID: 15942224

Prognosis

Auricchio L, Vitiello L, Adriani M, Ferri P, Chiocchetti A, Pettinato G, Racioppi L, Maiuri L, Dianzani U, Pignata C
Dermatology 2005;210(4):336-40. doi: 10.1159/000084762. PMID: 15942224

Clinical prediction guides

Marlies A, Udo G, Juergen B, Bernd S, Herrmann M, Haas JP
Autoimmunity 2007 Jun;40(4):299-301. doi: 10.1080/08916930701356473. PMID: 17516214

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