Stroke in patients with sickle cell anemia is multifactorial but occurs mainly by 2 mechanisms: occlusive arteriopathy and obliteration of small vessels with plugs of sickle cells. The high individual risk can be assessed by simple and well-defined strategies such as ultrasounds with transcranial and cervical Doppler Ultrasonography. The authors report the clinical case of a 25 year-old black female patient with sickle cell anemia, who was admitted with right hemiparesis. Cerebral MRI showed small recent fronto-temporo-parietal cortical-subcortical infarcts and several, older, posterior periventricular lacunae of left preponderance. A brief discussion is made, with particular emphasis on the proper treatment and prevention of its cere...
The most common cause of stroke in children with sickle cell anemia is infarction due to ischemia. I...
Abstract: Sickle cell disease is hereditary hemoglobinopathy which causes haemolytic anemia, vaso-oc...
Abstract – The aim of this study was to characterize a group of patients (n=8) with sickle cell dise...
Stroke, including asymptomatic cerebrovascular events, is a significant cause of morbidity and morta...
We describe a case of homozygous sickle cell anemia in which noninvasive transcranial Doppler ultras...
Stroke is a devastating and potentially fatal complication of sickle cell disease. The highest incid...
Cerebral infarction is a common complication of sickle cell disease and may manifest as overt stroke...
People with sickle cell disease, a chronic hemolytic anemia, present with a wide variety of neurolog...
The case of a patient with sickle cell disease is presented in which neuropsychological and magnetic...
Sickle cell disease, a chronic hemolytic anemia secondary to a single-gene mutation leading to a hem...
Sickle cell disease is an inherited blood disorder that affects red blood cells. It is characterized...
Neurologic complications are a major cause of morbidity and mortality in sickle cell disease (SCD). ...
Children with sickle cell disease, a chronic hemolytic anemia, present with a wide variety of neurol...
Children with sickle disease are at high risk for ischemic stroke and transient ischemic attacks, us...
Sickle cell disease (SCD) is a group of hemoglobinopathies that vary in severity, the most severe fo...
The most common cause of stroke in children with sickle cell anemia is infarction due to ischemia. I...
Abstract: Sickle cell disease is hereditary hemoglobinopathy which causes haemolytic anemia, vaso-oc...
Abstract – The aim of this study was to characterize a group of patients (n=8) with sickle cell dise...
Stroke, including asymptomatic cerebrovascular events, is a significant cause of morbidity and morta...
We describe a case of homozygous sickle cell anemia in which noninvasive transcranial Doppler ultras...
Stroke is a devastating and potentially fatal complication of sickle cell disease. The highest incid...
Cerebral infarction is a common complication of sickle cell disease and may manifest as overt stroke...
People with sickle cell disease, a chronic hemolytic anemia, present with a wide variety of neurolog...
The case of a patient with sickle cell disease is presented in which neuropsychological and magnetic...
Sickle cell disease, a chronic hemolytic anemia secondary to a single-gene mutation leading to a hem...
Sickle cell disease is an inherited blood disorder that affects red blood cells. It is characterized...
Neurologic complications are a major cause of morbidity and mortality in sickle cell disease (SCD). ...
Children with sickle cell disease, a chronic hemolytic anemia, present with a wide variety of neurol...
Children with sickle disease are at high risk for ischemic stroke and transient ischemic attacks, us...
Sickle cell disease (SCD) is a group of hemoglobinopathies that vary in severity, the most severe fo...
The most common cause of stroke in children with sickle cell anemia is infarction due to ischemia. I...
Abstract: Sickle cell disease is hereditary hemoglobinopathy which causes haemolytic anemia, vaso-oc...
Abstract – The aim of this study was to characterize a group of patients (n=8) with sickle cell dise...