Page last updated: 2024-10-26

brl 42810 and Wiskott-Aldrich Syndrome

brl 42810 has been researched along with Wiskott-Aldrich Syndrome in 1 studies

Wiskott-Aldrich Syndrome: A rare, X-linked immunodeficiency syndrome characterized by ECZEMA; LYMPHOPENIA; and, recurrent pyogenic infection. It is seen exclusively in young boys. Typically, IMMUNOGLOBULIN M levels are low and IMMUNOGLOBULIN A and IMMUNOGLOBULIN E levels are elevated. Lymphoreticular malignancies are common.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kim, JK1
Yoon, MS1
Huh, JY1
Kim, HJ1
Kim, DH1

Other Studies

1 other study available for brl 42810 and Wiskott-Aldrich Syndrome

ArticleYear
A novel mutation of the WAS gene in a patient with Wiskott-Aldrich syndrome presenting with recalcitrant viral warts.
    Journal of dermatological science, 2010, Volume: 60, Issue:2

    Topics: 2-Aminopurine; Acitretin; Adult; Antiviral Agents; Famciclovir; Humans; Kaposi Varicelliform Eruptio

2010