Homozygous Delta-Beta Thalassaemia With Alpha Thalassaemia and Erythrocytosis- a Rare Case Report

• Asıl Yazarlar: Hala Shokr (Yazar), Mandeep Kaur Marwah (Yazar), Hisam Siddiqi (Yazar), Christine Wright (Yazar), Sukhjinder Marwah (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Frontiers Media S.A., 2024-11-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

In this report, we describe a case of homozygous delta-beta (δβ) thalassaemia, a rare genetic disorder characterized by severe deficiency in delta (δ) and beta (β)-globin chain production, leading to ineffective erythropoiesis and chronic haemolytic anaemia. The patient, a 26-year-old female with δβ...