The Antley-Bixler syndrome: two new cases.

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dc.contributor.authorHosalkar, H Sen_US
dc.contributor.authorShah, H Sen_US
dc.contributor.authorGujar, P Sen_US
dc.contributor.authorShaw, B Aen_US
dc.date.accessioned2001-10-08en_US
dc.date.accessioned2009-06-02T11:44:13Z
dc.date.available2001-10-08en_US
dc.date.available2009-06-02T11:44:13Z
dc.date.issued2001-10-08en_US
dc.description12 references.en_US
dc.description.abstractThe 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.en_US
dc.description.affiliationDivision of Paediatric Orthopaedics, The Valley Children's Hospital, UCSF, California, USA. hosalkarish@hotmail.comen_US
dc.identifier.citationHosalkar HS, Shah HS, Gujar PS, Shaw BA. The Antley-Bixler syndrome: two new cases. Journal of Postgraduate Medicine. 2001 Oct-Dec; 47(4): 252-5en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/116422
dc.language.isoengen_US
dc.source.urihttps://www.jpgmonline.comen_US
dc.subject.meshAbnormalities, Multiple --geneticsen_US
dc.subject.meshContracture --geneticsen_US
dc.subject.meshCraniosynostoses --geneticsen_US
dc.subject.meshHumansen_US
dc.subject.meshInfanten_US
dc.subject.meshMaleen_US
dc.subject.meshMarfan Syndrome --geneticsen_US
dc.subject.meshSyndromeen_US
dc.subject.meshSynostosis --geneticsen_US
dc.titleThe Antley-Bixler syndrome: two new cases.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
dc.typeReviewen_US
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