Abstract:β-Thalassemia merupakan suatu kelainan genetik yang bersifat herediter dengan prevalensi tinggi di Asia Tenggara. Di Indonesia, diperkirakan sejumlah 200.000 bayi pembawa thalassemia lahir setiap tahun sehingga diperlukan upaya deteksi dini yang sederhana, cepat, dan murah. NESTROFT (Naked Eye Single Tube Red Cell Osmotic Fragility Test) sebagai metode deteksi berdasarkan fragilitas sel darah merah memiliki sensitivitas uji pada carrier β-thalassemia sebesar 99,8%. Oleh karena itu, pengembangan metode terseb… Show more
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