Publications by authors named "Bilgesu Ak"
Article Synopsis
- The study focuses on a case involving a 49-year-old woman diagnosed with rheumatoid arthritis and subsequent severe immune deficiency due to a homozygous mutation in the LRBA gene, which is crucial for immune regulation.
- The patient showed various symptoms, including massive splenomegaly, portal hypertension, and a rare type of cystitis associated with mast cells, indicating a complex clinical presentation.
- This case emphasizes the importance of understanding LRBA's role in immune function and the diverse clinical manifestations linked to its deficiency.
The present study described an extremely rare case of acute promyelocytic leukemia (APL) characterized by a complex three‑way (15;22;17)(q22;q11.2;q21) translocation. Acute promyelocytic leukemia (APL) is a specific subtype of acute myeloid leukemia with distinctive clinical and therapeutic characteristics.
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