Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area

Mohamad H. Qari, Yasser Wali, Muneer H. Albagshi, Mohammad Alshahrani, Azzah Alzahrani, Ibrahim A. Alhijji, Abdulkareem Almomen, Abdullah Aljefri, Hussain H. Al Saeed, Shaker Abdullah, Ahmad Al Rustumani, Khoutir Mahour, Shaker A. Mousa

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Thalassemia syndrome has diverse clinical presentations and a global spread that has far exceeded the classical Mediterranean basin where the mutations arose. The mutations that give rise to either alpha or beta thalassemia are numerous, resulting in a wide spectrum of clinical severity ranging from carrier state to life-threatening, inherited hemolytic anemia that requires regular blood transfusion. Beta thalassemia major constitutes a remarkable challenge to health care providers. The complications arising due to the anemia, transfusional iron overload, as well as other therapy-related complications add to the complexity of this condition. To produce this consensus opinion manuscript, a PubMed search was performed to gather evidence-based original articles, review articles, as well as published work reflecting the experience of physicians and scientists in the Arabian Gulf region in an effort to standardize the management protocol.

Original languageEnglish
Article number143
JournalOrphanet Journal of Rare Diseases
Volume8
Issue number1
DOIs
Publication statusPublished - 2013

Fingerprint

beta-Thalassemia
alpha-Thalassemia
Carrier State
Mutation
Iron Overload
Thalassemia
Manuscripts
Hemolytic Anemia
PubMed
Blood Transfusion
Health Personnel
Anemia
Physicians
Therapeutics

Keywords

  • Anemia
  • Arabian Gulf
  • Chelation
  • Iron chelation therapy
  • Iron overload
  • Thalassemia management
  • Transfusion

ASJC Scopus subject areas

  • Medicine(all)
  • Genetics(clinical)
  • Pharmacology (medical)

Cite this

Qari, M. H., Wali, Y., Albagshi, M. H., Alshahrani, M., Alzahrani, A., Alhijji, I. A., ... Mousa, S. A. (2013). Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area. Orphanet Journal of Rare Diseases, 8(1), [143]. https://doi.org/10.1186/1750-1172-8-143

Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area. / Qari, Mohamad H.; Wali, Yasser; Albagshi, Muneer H.; Alshahrani, Mohammad; Alzahrani, Azzah; Alhijji, Ibrahim A.; Almomen, Abdulkareem; Aljefri, Abdullah; Al Saeed, Hussain H.; Abdullah, Shaker; Al Rustumani, Ahmad; Mahour, Khoutir; Mousa, Shaker A.

In: Orphanet Journal of Rare Diseases, Vol. 8, No. 1, 143, 2013.

Research output: Contribution to journalArticle

Qari, MH, Wali, Y, Albagshi, MH, Alshahrani, M, Alzahrani, A, Alhijji, IA, Almomen, A, Aljefri, A, Al Saeed, HH, Abdullah, S, Al Rustumani, A, Mahour, K & Mousa, SA 2013, 'Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area', Orphanet Journal of Rare Diseases, vol. 8, no. 1, 143. https://doi.org/10.1186/1750-1172-8-143
Qari, Mohamad H. ; Wali, Yasser ; Albagshi, Muneer H. ; Alshahrani, Mohammad ; Alzahrani, Azzah ; Alhijji, Ibrahim A. ; Almomen, Abdulkareem ; Aljefri, Abdullah ; Al Saeed, Hussain H. ; Abdullah, Shaker ; Al Rustumani, Ahmad ; Mahour, Khoutir ; Mousa, Shaker A. / Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area. In: Orphanet Journal of Rare Diseases. 2013 ; Vol. 8, No. 1.
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