Related Experiment Video
Updated: Jan 25, 2026

Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Neurologic complications in children under five years with sickle cell disease
Aisha A Galadanci1, Michael R DeBaun2, Najibah A Galadanci3
1Department of Hematology and Blood Transfusion, Bayero University/Aminu Kano Teaching Hospital, Kano, Nigeria.
Insights
Neurologic complications, including silent cerebral infarct and cognitive impairment, are common in children under five with Sickle Cell Disease (SCD). Identifying and managing modifiable risk factors is crucial for preventing brain dysfunction in these young patients.
Area of Science:
- Pediatric Neurology
- Hematology
- Global Health
Background:
- Sickle Cell Disease (SCD) is a prevalent global genetic disorder impacting multiple organs.
- Preventing end-organ dysfunction, especially in the brain, is a significant challenge in managing pediatric SCD.
- Neurologic complications are frequent in children under five with SCD, including stroke, epilepsy, and encephalopathy.
Purpose of the Study:
- To review neurologic complications in children under five with SCD.
- To describe modifiable risk factors for these complications.
- To highlight differences in high versus low resource settings.
Main Methods:
- Literature search of the PubMed database.
- Utilized Medical Subject Headings (MeSH) and keywords.
- Focused on articles concerning neurologic complications in children under five with SCD.
Main Results:
- Silent cerebral infarct and cognitive impairment are the most common neurologic complications in young children with SCD.
- Neurologic complications may be underreported in this age group.
- Modifiable risk factors and disparities between resource settings were examined.
Conclusions:
- Neurologic complications in children under five with SCD are common and potentially underdiagnosed.
- Silent cerebral infarct and cognitive impairment are key concerns.
- Addressing modifiable risk factors is essential for improving outcomes in pediatric SCD.
Introduction:
Sickle Cell Disease (SCD) is one of the most common genetic diseases in the world affecting every organ. The major challenge in the medical care of children with SCD is preventing end-organ dysfunction, particularly the brain. Major neurologic complications in children less than five years with SCD include, but are not limited to, Silent cerebral infarct, cerebral sinus thrombosis, epilepsy, reversible encephalopathy syndrome, and ischemic and hemorrhagic stroke. Recurrent headaches and migraine are not rare in children under five years with SCD. This review will focus on the neurologic complications and the description of the modifiable risk factors in children less than 5 years of age with emphasis on differences between high and low resource settings.
Areas Covered:
Neurologic complications of children under 5 years of age and the modifiable risk factors. The PUBMED database was searched using medical subject headings (MeSH) and keywords for articles regarding neurologic complications in children under 5 years of age.
Conclusion:
Neurologic complications in children under five years of age with SCD may be more frequent than currently reported, among which Silent cerebral infarct and cognitive impairment are the most common.
Related Concept Videos
Chronic Obstructive Pulmonary Disease-III: Symptoms and Complications.
Symptoms of COPD can be classified as primary or systemic. Primary symptoms relate to reduced airflow, while systemic or extrapulmonary symptoms relate to COPD's broader impact on the body.
Primary Symptoms of COPD:
Hemodialysis II: Procedure and Complications
Diabetes: Symptoms, Diagnosis, and Complications
Pneumonia III: Complications and Assessment
Asthma-III: Symptoms and Complications
Classification of Asthma
Drug Dosing: Infants and Children

