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From the Department of Medical Genetics. University of South Alabama, School of Medicine. Medical University of South Carolina, and Children's Psychiatric Research Institute, London, Ontario
Abstract
The clinical syndrome associated with triploidy is quite typical but is rarely reported in near-term stillborns and new boms. The occurrence of a large placenta with areas of hydatidiform changes in combination with an edematous fetus with macroglossia, facial elefts, eye defects, dysplaslic cranial bones, omphalocele, meningomyelocele, syndactyly, and, in males, genital maldevelopment is suggestive of a triploid chromosomal constitution.
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