Outcome in hemoglobin SC disease: A four-decade observational study of clinical, hematologic, and genetic factors

Genetic and hematological studies in a g

Genetic and hematological studies in a group of 114 adult patients with SC sickle cell disease

✍ Lee, K.; Préhu, C.; Mérault, G.; Kéclard, L.; Roudot-Thoraval, F.; Bachir, D.; W 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 103 KB 👁 2 views

The clinical and biological heterogeneity of sickle cell hemoglobin (Hb) C disease (SC disease) is similar to sickle cell anemia, but has a much milder course. The effect of genetic factors such as ␣ thalassemia or ␤-globin gene haplotype has been analyzed in a limited number of cases. In this work,