Severe autoimmune lymphoproliferative syndrome phenotype in a pediatric patient with a germline FAS gene variant-Reference-Cited by-同舟云学术

Severe autoimmune lymphoproliferative syndrome phenotype in a pediatric patient with a germline FAS gene variant

Published:2023-03-28 Issue:7 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Dreyzin Alexandra¹^ORCID,Cheng Jinjun²,Leitenberg David³,Diab Yaser¹

Affiliation:

1. Center for Cancer and Blood Disorders Children's National Hospital Washington District of Columbia USA

2. Department of Pathology and Laboratory Medicine Children's National Hospital Washington District of Columbia USA

3. Department of Microbiology Immunology and Tropical Medicine The George Washington University School of Medicine and Health Sciences Washington District of Columbia USA

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30304

Reference16 articles.

1. Dominant interfering fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome

2. Autoimmune lymphoproliferative syndromes: genetic defects of apoptosis pathways

3. Autoimmune lymphoproliferative syndrome: more than a FAScinating disease

4. FAS-L, IL-10, and double-negative CD4−CD8− TCR α/β+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function

5. Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation

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