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March 3, 2024Hemoglobin

Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D HBA1: C. 119₁21delCCA Mutation and HBA2: C. *94A > G Mutation

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Authors

NANada AssafAmerican University of Beirut Medical CenterRZRoba El ZibaouiJohns Hopkins UniversityCMCarla MonsefAmerican University of Beirut Medical Center

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Cite This Study

Assaf et al. (2024) studied this question.

synapsesocial.com/papers/68e75efdb6db6435876d62c1https://doi.org/10.1080/03630269.2024.2338850
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Genetic Analysis of Two Patients with Compound Thalassemia Presenting with Elevated HbF and Normal HbA <sub>2</sub> Levels2026
  2. 2A Compound Heterozygous of Hb E and Beta Thalassemia Independent of Transfusion: A Rare Case Report2024
  3. 3Premarital Counseling on the Alpha Thalassemia Allele HBA2:c.*94A&gt;G2024
  4. 4Microcytic Anemia with Low HbA 2 and Normal HbA: Two Cases of Rare Thalassemia2026
  5. 5α-globin gene 20.5kb deletion and triplication mutations among Palestinian patients with microcytic hypochromic anemia2025