A diagnostic dilemma in AL(L)PS

Ann Hematol. 2014 Mar;93(3):515-6. doi: 10.1007/s00277-013-1823-0. Epub 2013 Jun 20.

Authors

Cariosa Lee-Brennan¹, Maeve O'Reilly, Owen Smith, John Quinn, Philip Murphy, Mary Keogan

Affiliation

¹ Department of Immunology, Beaumont Hospital, Beaumont, Dublin 9, Ireland.

PMID: 23783422
DOI: 10.1007/s00277-013-1823-0

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Anemia / etiology
Autoimmune Lymphoproliferative Syndrome / diagnosis*
Autoimmune Lymphoproliferative Syndrome / genetics*
Autoimmune Lymphoproliferative Syndrome / physiopathology
Autoimmune Lymphoproliferative Syndrome / therapy
Codon, Nonsense
Delayed Diagnosis
Disease Progression
Exons
Family Health
Fathers
Female
Hepatomegaly / etiology
Humans
Infant
Lymphatic Diseases / etiology
Precursor Cell Lymphoblastic Leukemia-Lymphoma / diagnosis
Splenomegaly / etiology
Thrombocytopenia
fas Receptor / genetics*
fas Receptor / metabolism

Substances

Codon, Nonsense
FAS protein, human
fas Receptor