AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME (ALPS)-A RARE CASE WITH COMMON CLINICAL MANIFESTATION

2015 ◽  
Vol 12 (1) ◽  
Author(s):  
Abhilasha Sampagar ◽  
S M Jali ◽  
Prakash R Malur ◽  
Mallikarjun Jali
Keyword(s):  
Clinical Manifestation ◽  
Rare Case ◽  
Autoimmune Lymphoproliferative Syndrome ◽  
Common Clinical Manifestation ◽  
Lymphoproliferative Syndrome

scholarly journals Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations

Blood ◽  
2014 ◽  
Vol 123 (13) ◽  
pp. 1989-1999 ◽  
Author(s):  
Susan Price ◽  
Pamela A. Shaw ◽  
Amy Seitz ◽  
Gyan Joshi ◽  
Joie Davis ◽  
...  
Keyword(s):  
Natural History ◽  
Clinical Manifestation ◽  
Gene Mutations ◽  
Morbidity And Mortality ◽  
Carrier Rate ◽  
Autoimmune Lymphoproliferative Syndrome ◽  
Key Points ◽  
History Of ◽  
High Carrier ◽  
Lymphoproliferative Syndrome

Key Points Less than 60% of individuals who inherit a FAS mutation have a clinical manifestation of ALPS, implying a high carrier rate. Major causes of morbidity and mortality in ALPS patients are sepsis following splenectomy and development of lymphoma.

scholarly journals Rare CVID-like phenotype of autoimmune lymphoproliferative syndrome

2021 ◽  
Vol 20 (1) ◽  
pp. 170-179
Author(s):  
O. A. Shvets ◽  
E. A. Deordieva ◽  
M. A. Kurnikova ◽  
D. E. Pershin ◽  
A. M. Kieva ◽  
...  
Keyword(s):  
Immune Deficiency ◽  
Primary Immunodeficiency ◽  
Rare Case ◽  
Scientific Research ◽  
Common Variable Immune Deficiency ◽  
Autoimmune Lymphoproliferative Syndrome ◽  
Timely Diagnosis ◽  
Lymphoproliferative Syndrome ◽  
Common Variable

Autoimmune lymphoproliferative syndrome is a primary immunodeficiency caused by defective FAS-mediated apoptosis and usually accompanied by hypergammaglobulinemia. Yet some exceptions take place in the cohort of patients that complicated timely diagnosis, in particular, some symptoms may resemble common variable immune deficiency. In this article, we describe the patient with rare case of agammaglobulinemia and genetically confirmed autoimmune lymphoproliferative syndrome. The patient's parents agreed to use the information, including the child's photo, in scientific research and publications. 

Bilateral uveitis in a patient with autoimmune lymphoproliferative syndrome

2005 ◽  
Vol 139 (3) ◽  
pp. 562-563 ◽  
Author(s):  
Wee-Kiak Lim ◽  
Roxana Ursea ◽  
Koneti Rao ◽  
Ronald R. Buggage ◽  
Eric B. Suhler ◽  
...  
Keyword(s):  
Autoimmune Lymphoproliferative Syndrome ◽  
Lymphoproliferative Syndrome

scholarly journals Autoimmune Pancreatitis in the Autoimmune Lymphoproliferative Syndrome (ALPS)

Pancreas ◽  
2013 ◽  
Vol 42 (2) ◽  
pp. 363-366 ◽  
Author(s):  
Russell C. Langan ◽  
Fred Gill ◽  
Manish T. Raiji ◽  
John E. Mullinax ◽  
Stefania Pittaluga ◽  
...  
Keyword(s):  
Autoimmune Pancreatitis ◽  
Autoimmune Lymphoproliferative Syndrome ◽  
Lymphoproliferative Syndrome
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