X-linked lymphoproliferative (XLP) syndrome comprises rare immunodeficiencies resulting from mutations in the SH2D1A (XLP1) or XIAP (XLP2) gene, typically leading to overwhelming Epstein–Barr virus infection and sometimes lymphomas in boys.
El síndrome de linfoproliferación ligado al cromosoma X (XLP) son enfermedades raras por mutaciones en SH2D1A (XLP1) o XIAP (XLP2), que causan infecciones graves por EBV y linfomas en niños.
| Front | Rare immunodeficiency diseases that result from mutations in the gene, SH2D1A, XLP1 or, XIAP, XLP2. Boys with this deficiency typically develop overwhelming Epstein–Barr virus infection during childhood, and sometimes lymphomas |
|---|---|
| Back | X-linked lymphoproliferative XLP syndrome |
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