HASPESLAGH SYNDROME WITHOUT SEVERE MENTAL-RETARDATION AND PTERYGIA

An adult female is described with mild developmental delay, typical fa cies, dental anomalies, arachnodactyly and camptodactyly. In many resp ects she resembles four other patients described earlier; but differs in not having multiple pterygia, nor severe mental retardation. We sug gest that this entity should be named Haspeslagh syndrome. The differe ntial diagnosis is discussed.