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J Postgrad Med ; 2001 Oct-Dec; 47(4): 252-5
Article in English | IMSEAR | ID: sea-116422

ABSTRACT

The Antley-Bixler syndrome is a rare multiple congenital anomaly with a high mortality rate. The characteristic manifestations include craniosynostosis, radiohumeral synostosis, midface hypoplasia, joint contractures and arachnodactyly. We report two new cases of this syndrome and address the diagnostic features, associated malformations, inheritance patterns, prenatal findings, and briefly review the literature.


Subject(s)
Abnormalities, Multiple/genetics , Contracture/genetics , Craniosynostoses/genetics , Humans , Infant , Male , Marfan Syndrome/genetics , Syndrome , Synostosis/genetics
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