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Clinical, Radiological, and Demographic Details of Benign External Hydrocephalus: A Population-Based Study
Sverre Morten Zahl1, Arild Egge2, Eirik Helseth3
1Department of Clinical Medicine K1, University of Bergen, Norway; Department of Ear, Nose and Throat, Aalesund Hospital, Aalesund, Norway.
Benign external hydrocephalus (BEH) in infants typically presents with a normal head circumference at birth, rapidly increasing before six months. This condition, affecting mostly boys, often shows normalized neuroimaging by 12 months.
Area of Science:
- Pediatric Neurology
- Neuroradiology
- Infant Health
Background:
- Benign external hydrocephalus (BEH) affects approximately 0.4 per 1000 live births.
- Characterized by rapid head circumference increase and specific neuroimaging findings in infants.
- Previous studies often involved small, selected patient groups, limiting generalizability.
Purpose of the Study:
- To report on the incidence and characteristics of benign external hydrocephalus (BEH).
- To follow up on a recently published study on BEH incidence.
- To analyze a large, population-based cohort for a comprehensive understanding of BEH.
Main Methods:
- Retrospective, population-based study across two Norwegian health regions (1994-2003).
- Inclusion criteria: infants with increasing head circumference and typical radiological findings of enlarged subarachnoid spaces.
- Data collected: head circumference, neuroimaging, delivery methods, and demographics from medical records.
Main Results:
- 176 infants diagnosed with BEH; 86.4% were male.
- Abnormal head circumference typically developed by 3.4 months (range: birth to 7 months).
- Most infants (80%) had dilated lateral ventricles alongside enlarged subarachnoid spaces; neuroimaging normalized by 12 months for many.
Conclusions:
- Infants with BEH usually have normal head circumference at birth, with rapid enlargement before six months.
- The age and gender distribution of BEH mirrors that of infant subdural hemorrhage.
- Findings suggest a distinct pattern of rapid head growth in BEH, distinct from other causes of macrocephaly.
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