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Haspeslagh syndrome without severe mental retardation and pterygia?
1Institute of Human Genetics, University of Amsterdam, The Netherlands.
Clinical Genetics
|May 1, 1995
Abstract:
An adult female is described with mild developmental delay, typical facies, dental anomalies, arachnodactyly and camptodactyly. In many respects she resembles four other patients described earlier, but differs in not having multiple pterygia, nor severe mental retardation. We suggest that this entity should be named Haspeslagh syndrome. The differential diagnosis is discussed.