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Published on: April 8, 2019
Congenital brain malformations in Sudanese children: an outpatient-based study
Inaam Noureldyme Mohammed1, Soad Abdalaziz Suliman2, Maha A Elseed1
1Department of Paediatrics and Child Health, Faculty of Medicine, University of Khartoum, Sudan.
Insights
Congenital brain malformations (CBMs) affect 5% of pediatric neurology patients in Sudan. Cortical malformations were the most frequent type observed in this study.
Area of Science:
- Neurology
- Developmental Biology
- Pediatrics
Background:
- Congenital brain malformations (CBMs) are diverse structural abnormalities of the developing brain.
- Etiologies include prenatal infections, teratogens, and genetic factors.
- High consanguinity rates and potential for prenatal infections suggest CBMs may be prevalent in Sudan.
Purpose of the Study:
- To review the clinical characteristics of children diagnosed with CBMs.
- To identify the common types of CBMs in Sudanese children.
- To assess the frequency of CBMs in pediatric neurology clinics in Khartoum State, Sudan.
Main Methods:
- Clinical evaluation and neuroimaging were used to diagnose CBMs.
- Patients under 18 with developmental delay, seizures, or abnormal head size were included.
- Data was collected over six months (September 2016-March 2017) from two tertiary pediatric neurology clinics.
Main Results:
- 105 out of 2,114 patients (5%) were diagnosed with CBMs.
- The majority of patients had single (57.1%) or multiple (42.9%) brain anomalies.
- Cortical malformations were the most common CBMs, observed in 35.1% of cases.
Conclusions:
- CBMs represent a significant neurological condition in Sudanese children.
- Cortical malformations are the predominant type of CBMs.
- Further community-based studies are necessary to determine CBM prevalence, causes, and outcomes in Sudan.
Abstract:
Congenital brain malformations (CBMs) are a heterogeneous group characterised by abnormal structure of the developing brain. Their aetiology includes in-utero infections, teratogenicity and in a considerable group, genetic causes. Due to the high rate of consanguineous marriages and the possible high prevalence of prenatal infections in Sudan, CBMs are likely to be common. The main aim of this study was to review the clinical profile of children with CBMs attending two main tertiary paediatrics neurology outpatient clinics in Khartoum State, Sudan. Children under the age of 18 years who presented with developmental delay, seizures or abnormal head size were evaluated clinically and with neuroimaging for possible CBMs. Out of 2,114 patients seen within 6 months (September 2016-March 2017) at the Outpatient Departments, 105 patients (5%) were diagnosed with CBMs. Sixty patients (57.1%) had a single brain anomaly, 36 patients (34.1%) had two brain anomalies while nine patients (8.6%) had multiple brain anomalies. Collectively, cortical malformations either isolated or in combination with other anomalies were observed in 37 patients (35.1%), thus by representing the commonest CBMs. Community-based epidemiological studies are needed to ascertain CBMs prevalence, common causes and long-term outcomes.
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