scholarly journals Spina bifida: early antenatal diagnosis using amniotic fluid alpha-fetoprotein heterogeneity.

BMJ ◽  
1979 ◽  
Vol 2 (6202) ◽  
pp. 1402-1403 ◽  
Author(s):  
D J Brock
The Lancet ◽  
1974 ◽  
Vol 303 (7855) ◽  
pp. 429-433 ◽  
Author(s):  
R. Harris ◽  
R.F. Jennison ◽  
A.J. Barson ◽  
K.M. Laurence ◽  
E. Ruoslahti ◽  
...  

The Lancet ◽  
1973 ◽  
Vol 302 (7828) ◽  
pp. 522-525 ◽  
Author(s):  
LindseyD. Allan ◽  
Ian Donald ◽  
M.A. Ferguson-Smith ◽  
ElizabethM. Sweet ◽  
A.A.M. Gibson

The Lancet ◽  
1973 ◽  
Vol 301 (7813) ◽  
pp. 1187 ◽  
Author(s):  
J. Lorber ◽  
C.R. Stewart ◽  
A. Milford Ward

1981 ◽  
Vol 27 (10) ◽  
pp. 1658-1660 ◽  
Author(s):  
P K Buamah ◽  
P Taylor ◽  
A M Ward

Abstract Concanavalin A nonreactive alpha-fetoprotein was determined in samples of amniotic fluid from 16 abnormal pregnancies complicated by anencephaly (7), open spina bifida (6), intra-uterine death (1), anencephaly with exomphalos (1), or open spina bifida with exomphalos (1), and in amniotic fluid from 50 normal pregnancies with gestational age between 13 and 24 weeks. In all 16 cases with fetal malformations, the proportion of nonreactive alpha-fetoprotein was significantly decreased (median 5.3%) as compared with amniotic fluid from pregnancies with a normal outcome (median 39.7%). The results confirm that this measurement is useful in the diagnosis of neural tube defects, especially when the concentration of alpha-fetoprotein in amniotic fluid is normal or only slightly above normal and gestational age is uncertain.


The Lancet ◽  
1972 ◽  
Vol 300 (7770) ◽  
pp. 197-199 ◽  
Author(s):  
D.J.H Brock ◽  
R.G Sutcliffe

1975 ◽  
Vol 12 (2) ◽  
pp. 135-137 ◽  
Author(s):  
G R Sutherland ◽  
D J Brock ◽  
J B Scrimgeour

PEDIATRICS ◽  
1974 ◽  
Vol 53 (3) ◽  
pp. 307-308
Author(s):  
John Lorber

There never was and perhaps never will be a really satisfactory method of treatment for infants born with severe myelomeningocele, nor for the management of their families, in spite of the best technical advances and the most humane attempts. The best hope for the future lies in prevention of conception of such infants, but we are far from that. The next best hope is early antenatal diagnosis so that at least we can prevent the birth of such infants. The recent discovery that abnormally high levels of alpha-fetoprotein are present in the amniotic fluid of women carrying an infant with spinal or cranial dysraphism has already been put to routine practical use.


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