Craniosynostosis,Philadelphia type: A new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toes |
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Authors: | Nathaniel H. Robin Barbara Segel Gary Carpenter Maximilian Muenke |
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Affiliation: | The Children's Hospital of Philadelphia, Division of Human Genetics and Molecular Biology |
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Abstract: | The acrocephalosyndactyly syndromes (ACS) are a group of clinically similar disorders that share the manifestations of craniosynostosis and a variety of hand and foot anomalies. Here we report on a 5-generation kindred segregating sagittal craniosynostosis and syndactyly of the fingers and the toes in an autosomal dominant manner. The anomalies seen in this kindred comprise a syndrome distinct from other craniosynostosis syndromes. For this novel syndrome, we propose the name craniosynostosis, Philadelphia type. © 1996 Wiley-Liss, Inc. |
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Keywords: | craniosynostosis syndactyly acrocephalosyndactyly |
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