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P02.71: Prenatal diagnosis of Meckel-Gruber syndrome

✍ Scribed by M. Rasidaki; M. Papadaki; S. Mitas; N. Paikopoulos; J. Stratakis; G. Kouvidis


Book ID
112225156
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
38 KB
Volume
28
Category
Article
ISSN
0960-7692

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Prenatal diagnosis of Meckel syndrome
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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

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