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Acute chest syndrome in sickle cell disease/HBE patient, A case report
  • Ibrahim Khamees,
  • mohamed yassin,
  • Waail Rozi
Ibrahim Khamees

Corresponding Author:[email protected]

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mohamed yassin
HMC NCCCR
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Waail Rozi
Hamad Medical Corporation
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Abstract

Hemoglobin S (HBS) and hemoglobin E (HBE) are common hemoglobinopathies, but combined heterozygosity of HBS and HBE (HBSE) is relatively a rare disease. Most reports suggest that HBSE is generally benign condition. In this report we describe a 17-year-old male patient presenting with acute chest syndrome treated with exchange transfusion.

Peer review status:Published

02 Nov 2020Submitted to Clinical Case Reports
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12 Dec 2020Submission Checks Completed
12 Dec 2020Assigned to Editor
25 Jan 2021Reviewer(s) Assigned
10 Feb 2021Review(s) Completed, Editorial Evaluation Pending
13 Feb 2021Editorial Decision: Revise Minor
25 Feb 20211st Revision Received
25 Feb 2021Submission Checks Completed
25 Feb 2021Review(s) Completed, Editorial Evaluation Pending
25 Feb 2021Assigned to Editor
25 Feb 2021Reviewer(s) Assigned
02 Jun 2021Editorial Decision: Revise Minor
03 Jun 20212nd Revision Received
04 Jun 2021Assigned to Editor
04 Jun 2021Submission Checks Completed
04 Jun 2021Review(s) Completed, Editorial Evaluation Pending
16 Jun 2021Editorial Decision: Accept
Aug 2021Published in Clinical Case Reports volume 9 issue 8. 10.1002/ccr3.4575