𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Roentgenologic features of the Meckel syndrome

✍ Scribed by U. Seppänen; R. Herva


Book ID
105258258
Publisher
Springer-Verlag
Year
1983
Tongue
English
Weight
726 KB
Volume
13
Category
Article
ISSN
0301-0449

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Prenatal diagnosis of Meckel syndrome
✍ Nico J. Leschot; Jaak J. Nef; Mies J. Becker-Bloemkolk; Marianne Verjaal; Paul F 📂 Article 📅 1978 🏛 Springer 🌐 English ⚖ 183 KB

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

The meckel syndrome in the Hutterites
✍ Schurig, Verena ;Bowen, Peter ;Harley, Frances ;Schiff, David ;Opitz, John M. 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 English ⚖ 574 KB
Dandy-Walker malformation in the Meckel
✍ Herriot, Richard ;Hallam, Lavinia A. ;Gray, Elizabeth S. 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 476 KB 👁 2 views

The Meckel syndrome is an autosomal recessive condition and includes a heterogeneous group of CNS malformations, most frequently occipital encephalocele. We report on 2 sibs and one other unrelated case with Meckel syndrome in whom the CNS anomaly was the Dandy-Walker malformation, an association no

Dandy-Walker malformation in the Meckel
✍ Summers, Michael C. ;Donnenfeld, Alan E. 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 555 KB

## Abstract The Meckel syndrome (MS) is an autosomal recessive disorder classically defined by the triad of occipital encephalocele, multicystic kidneys, and polydactyly. Here we describe 3 sibs with varying manifestations of MS. The propositus had isolated cystic renal disease. The other sibs were