SC Hemoglobinopathy: a rare case report

In SC hemoglobinopathy, a rare type of sickle cell disease, patients may experience vaso-occlusive phenomena, but in milder condition than the SS form, considered classic and most common among them. This current study aims to present case patient with this form who received late diagnosis, its clinical evolution, including symptoms, treatment life expectancy based on literature, mainly how is clinically found after seven years follow-up. It important have epidemiological studies about hemoglobinopathies, specially forms, obtain more information regarding incidence/prevalence disease manifestations.