Paroxysmal Nocturnal Hemoglobinuria with a Distinct Molecular Signature Diagnosed Ten Years after Allogenic Bone Marrow Transplantation for Acute Myeloid Leukemia
Paroxysmal nocturnal hemoglobinurea (PNH) is a rare disorder of complement regulation due to somatic mutation of PIGA (phosphatidylinositol glycan anchor) gene. We herewith report a case who developed a symptomatic PNH long after an allogenic marrow transplant. Some reasonable arguments concerning t...
Saved in:
| Main Authors: | Alberto Santagostino, Laura Lombardi, Gerard Dine, Pierre Hirsch, Srimanta Chandra Misra |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wiley
2019-01-01
|
| Series: | Case Reports in Hematology |
| Online Access: | http://dx.doi.org/10.1155/2019/8928623 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Treatment of paroxysmal nocturnal hemoglobinuria
by: I. A. Lisukov, et al.
Published: (2014-07-01) -
Paroxysmal nocturnal hemoglobinuria: Pandora’s box?
by: Mihnea-Alexandru Găman, et al.
Published: (2020-10-01) -
Paroxysmal nocturnal hemoglobinuria: the path to diagnosis
by: E. F. Makhnyr, et al.
Published: (2019-04-01) -
The Advancing Landscape of Paroxysmal Nocturnal Hemoglobinuria Treatment
by: Cameron Perry, et al.
Published: (2025-06-01) -
A case of paroxysmal nocturnal hemoglobinuria with renal hemosiderosis
by: Parimal B Patel, et al.
Published: (2019-01-01)