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Fetal head shape in spina bifida in the second trimester.
M E Furness1, J E Barbary, P W Verco
1Department of Radiology, Queen Victoria Hospital, Adelaide, Australia.
Journal of Clinical Ultrasound : JCU
|September 1, 1987
Summary
A specific fetal head shape, characterized by anterior cranial narrowing without oligohydramnios, signals a potential risk for spina bifida. This finding necessitates further spinal and cerebellar evaluation in the second trimester.
Area of Science:
- Prenatal diagnosis
- Fetal medicine
- Medical imaging
Background:
- Spina bifida is a complex neural tube defect with significant long-term implications.
- Early detection of fetal anomalies is crucial for timely intervention and management.
- Ultrasonography is a primary tool for prenatal screening and diagnosis.
Purpose of the Study:
- To identify and describe a specific ultrasonographic finding indicative of potential spina bifida.
- To highlight the significance of anterior cranial narrowing in the absence of oligohydramnios as a warning sign.
- To emphasize the need for comprehensive fetal assessment upon detecting this anomaly.
Main Methods:
- Retrospective analysis of second-trimester fetal ultrasound examinations.
- Identification of cases with anterior cranial narrowing near the coronal sutures.
- Exclusion of cases with oligohydramnios.
- Correlation of ultrasonographic findings with confirmed diagnoses.
Main Results:
- Unequivocal anterior cranial narrowing, particularly around the coronal sutures, was observed as a potential marker.
- This finding, in the absence of oligohydramnios, was associated with an increased risk of spina bifida.
- The presence of this cranial anomaly prompted further detailed examination of the fetal spine and cerebellum.
Conclusions:
- Anterior cranial narrowing without oligohydramnios serves as a critical warning sign for spina bifida in the second trimester.
- This ultrasonographic feature mandates a thorough evaluation of the fetal spine, cerebellum, and other relevant structures.
- Amniocentesis may be considered for genetic assessment and further diagnostic confirmation.