glycine 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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Rottem, M | 1 |
| Alon-Shalev, S | 1 |
| Shneor, Y | 1 |
| Hujeirat, Y | 1 |
1 other study available for glycine and Wiskott-Aldrich Syndrome
| Article | Year |
|---|---|
Wiskott Aldrich syndrome in an Israeli family: identification of a novel G40V mutation.
Topics: Amino Acid Substitution; Child, Preschool; Glycine; Humans; Infant; Jews; Male; Mutation, Missense; | 2000 |