Nalaganje...
Bone marrow necrosis and fat embolism syndrome: a near fatal complication in previously undiagnosed sickle beta + thalassaemia
Prevalence of haemoglobin sickle-β(+) thalassaemia (Hb S/β+thal) is variable with geography ranging from 0.2% to 10% among sickle cell patients. Clinical presentation of Hb S/β+thal patients depends on HbA level, with milder disease often going undiagnosed. However, rarely these patients can present...
Shranjeno v:
| izdano v: | BMJ Case Rep |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BMJ Publishing Group
2021
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7789434/ https://ncbi.nlm.nih.gov/pubmed/33408108 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2020-238317 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|