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pubmed-article:12150214pubmed:dateCreated2002-8-1lld:pubmed
pubmed-article:12150214pubmed:abstractTextIn this report we describe a 17 weeks old female fetus with a lumbosacral meningocoele, multicystic renal dysplasia (Potter type IIb) and postaxial polydactyly type A at the left hand and left foot. There was no hepatic fibrosis. Although multicystic renal dysplasia and postaxial polydactyly are often present in the Meckel syndrome, a lumbosacral neural tube defect is not a typical finding in this syndrome.lld:pubmed
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pubmed-article:12150214pubmed:pagination147-9lld:pubmed
pubmed-article:12150214pubmed:dateRevised2006-7-6lld:pubmed
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pubmed-article:12150214pubmed:year2002lld:pubmed
pubmed-article:12150214pubmed:articleTitleMultiple congenital anomalies syndrome with multicystic renal dysplasia, postaxial polydactyly and lumbosacral meningocoele. Difficulties in nosological classification and genetic counseling.lld:pubmed
pubmed-article:12150214pubmed:affiliationDepartment of Obstetrics and Gynecology, University of Leuven, Belgium.lld:pubmed
pubmed-article:12150214pubmed:publicationTypeJournal Articlelld:pubmed