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 syndrome
β Scribed by Summers, Michael C. ;Donnenfeld, Alan E.
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 555 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0148-7299
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β¦ Synopsis
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 both prenatally diagnosed with renal disease, polydactyly, and the DandyβWalker malformation, an unusual central nervous system defect in MS. These findings are discussed in the context of the phenotypic expression of MS and the nosology of this disorder and the cerebroβrenoβdigital (Meckelβlike) syndromes. Β© 1995 WileyβLiss, Inc.
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