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Article in English | IMSEAR | ID: sea-86162

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/classification , Adult , Cerebral Ventricles/abnormalities , Craniofacial Dysostosis/classification , Diagnosis, Differential , Humans , India , Male , Tomography, X-Ray Computed
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