| Literature DB >> 81169 |
N J Leschot, J J de Nef, M J Becker-Bloemkolk, M Verjaal, P F Wiesenhaan.
Abstract
The three main features of Meckel syndrome are encephalocele, polycystic kidneys, and polydactyly. Prenatal diagnosis of a fetus with Meckel syndrome was made in the 16th week of gestation by means of amniotic fluid alpha1 fetoprotein estimation. The indication for amniocentesis was a previous child with an occipital meningocele and polycystic kidneys. Interpretation of the alpha1-fetoprotein value (240 microgram/ml) was difficult due to fetal blood contamination. Prenatal diagnosis is indicated in any pregnancy following the birth of a child with only two major symptoms of Meckel syndrome.Entities:
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Year: 1978 PMID: 81169 DOI: 10.1007/BF00278842
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132