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Published in: Child's Nervous System 7-8/2003

01-08-2003 | Original Paper

Prenatal biochemical screening for neural tube defects

Author: Françoise Muller

Published in: Child's Nervous System | Issue 7-8/2003

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Abstract

Introduction

Neural tube defects (NTDs) can be considered as a folate deficiency disorder. The prevalence of NTDs ranges from about 0.5 to 6 in 1,000 births.

Discussion

Two steps can be distinguished in biochemical screening for NTDs: 1. Screening in the general population, which is based on two complementary methods, maternal serum AFP screening and ultrasound screening; 2. Screening in a high-risk group, which requires fetal scanning by an expert sonographer.

Conclusion

Amniocentesis for acetylcholinesterase electrophoresis is indicated when sonographic scans are difficult to interpret.
Literature
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go back to reference Wald NJ, Cuckle H, Nanchahal K (1989) Amniotic fluid acetylcholinesterase measurement in the prenatal diagnosis of open neural tube defects. Second Report of the Collaborative Acetylcholinesterase Study. Prenat Diagn 9:813–829PubMed Wald NJ, Cuckle H, Nanchahal K (1989) Amniotic fluid acetylcholinesterase measurement in the prenatal diagnosis of open neural tube defects. Second Report of the Collaborative Acetylcholinesterase Study. Prenat Diagn 9:813–829PubMed
Metadata
Title
Prenatal biochemical screening for neural tube defects
Author
Françoise Muller
Publication date
01-08-2003
Publisher
Springer-Verlag
Published in
Child's Nervous System / Issue 7-8/2003
Print ISSN: 0256-7040
Electronic ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-003-0784-3

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