Publications by authors named "Samia Emad Al Saddik"
Ann Med Surg (Lond)
June 2024
Article Synopsis
- Alpha thalassemia, especially from nondeletional mutations, often leads to severe clinical outcomes, making DNA testing essential for diagnosing carriers, especially if they show minor hematological issues.*
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- A case study highlights a 1-year-old girl with a rare alpha-thalassemia genotype featuring both Hb Adana and Hb SEA, showing the importance of understanding these uncommon combinations.*
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- The authors emphasize the need for genetic evaluations and awareness of genotype-phenotype correlations to aid in managing alpha thalassemia, and they advocate for increased research and early screening to improve patient outcomes.*
