The meckel syndrome in the Hutterites
β Scribed by Schurig, Verena ;Bowen, Peter ;Harley, Frances ;Schiff, David ;Opitz, John M.
- Book ID
- 102698971
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 574 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0148-7299
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π SIMILAR VOLUMES
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
## 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