loading page

Moyamoya Syndrome in a Child with HbEβ-Thalassemia
  • +1
  • Akmal Zahra,
  • Hanan Al-Abboh,
  • Yousif Habeeb,
  • Adekunle Adekile
Akmal Zahra
Mubarak Al-Kabeer Hospital

Corresponding Author:[email protected]

Author Profile
Hanan Al-Abboh
Mubarak Al-Kabeer Hospital
Author Profile
Yousif Habeeb
Mubarak Al-Kabeer Hospital
Author Profile
Adekunle Adekile
Kuwait University
Author Profile

Abstract

Moyamoya is a progressive cerebrovascular disease associated with stenosis or occlusion of the arteries of the Circle of Willis. It is uncommon in thalassemia. We present a 9-year-old girl, with HbEβ-thalassemia, who presented with headache, vomiting and episodes of transient hemiparesis with complete occlusion internal carotid arteries.
27 Sep 2021Submitted to Clinical Case Reports
28 Sep 2021Submission Checks Completed
28 Sep 2021Assigned to Editor
01 Dec 2021Reviewer(s) Assigned
04 Jan 2022Review(s) Completed, Editorial Evaluation Pending
04 Jan 2022Editorial Decision: Revise Minor
03 Feb 20221st Revision Received
11 Feb 2022Submission Checks Completed
11 Feb 2022Assigned to Editor
11 Feb 2022Review(s) Completed, Editorial Evaluation Pending
20 Feb 2022Editorial Decision: Accept
Mar 2022Published in Clinical Case Reports volume 10 issue 3. 10.1002/ccr3.5536