Haspeslagh syndrome without severe mental retardation and pterygia?

Y. van Bever, R. C. Hennekam

Research output: Contribution to journalComment/Letter to the editorAcademic

2 Citations (Scopus)

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
Original languageEnglish
Pages (from-to)263-266
JournalClinical genetics
Volume47
Issue number5
Publication statusPublished - 1995

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