Publications by authors named "Mohammed T Aqeel"
Case Rep Hematol
December 2021
Article Synopsis
- Hemophagocytic lymphohistiocytosis (HLH) is a severe inflammatory syndrome that can lead to organ failure and death, with symptoms like high fever and blood issues.
- A case study details a 17-year-old male with G6PD deficiency experiencing prolonged fever and neurological symptoms, ultimately leading to a diagnosis of familial HLH type 2 with central nervous system involvement.
- Following treatment with immunosuppressive drugs, the patient showed significant improvement, emphasizing the need for prompt diagnosis and intervention in similar cases, especially in communities with high consanguinity rates.
