Serarslan, GamzeMelek, Ismet MuratAkgül, FeritSerarslan, YurdalDuman, Taşkin2024-09-192024-09-1920061301-1375https://hdl.handle.net/20.500.12483/15205Sickle cell disease is an inherited hemoglobinopathy and polymerization of deoxygenated HbS lead to clinical manifestations of the disease. The stroke rate in sickle cell disease patients with silent cerebral infarct is 14-fold higher than in those with normal MRI. We present two patients of sickle cell disease with leg ulcer, pulmonary hypertension and silent cerebral infarct and the only symptom was the leg ulcer.eninfo:eu-repo/semantics/closedAccessLeg ulcerPulmonary hypertensionSickle cell diseaseSilent cerebral infarctLeg ulcer, pulmonary hypertension and silent cerebral infarct in two patients with sickle cell diseaseArticle12389912-s2.0-33846392588N/A