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J Assoc Physicians India ; 48(8): 842-4, 2000 Aug.
Article in English | MEDLINE | ID: mdl-11273485

ABSTRACT

A rare variant of Apert syndrome having overlapping features of Crouzon syndrome is described. The salient features of the two syndromes are briefly discussed and overlapping features are highlighted. A possible genetic explanation for the same is mentioned.


Subject(s)
Acrocephalosyndactylia/diagnosis , Craniofacial Dysostosis/diagnosis , Acrocephalosyndactylia/classification , Acrocephalosyndactylia/genetics , Adult , Cerebral Ventricles/abnormalities , Cerebral Ventricles/pathology , Craniofacial Dysostosis/classification , Craniofacial Dysostosis/genetics , Diagnosis, Differential , Humans , India , Male , Tomography, X-Ray Computed
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