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Prenatal diagnosis of type 2 Pfeiffer syndrome

✍ Scribed by Dr P. S. Bernstein; S. J. Gross; D. J. Cohen; G. R. Tiller; A. L. Shanske; A. T. Bombard; R. W. Marion


Book ID
114433525
Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
477 KB
Volume
8
Category
Article
ISSN
0960-7692

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We report on the occurrence of Pfeiffer-type cardiocranial syndrome in a brother and sister born to unaffected parents. The cardinal manifestations of the syndrome are congenital heart defect, sagittal craniosynostosis, genital anomalies, and mental and growth retardation. The craniosynostosis was p