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Crouzon syndrome: A case report and review of literature

Crouzon syndrome, also called craniofacial dysostosis is an autosomal dominant disorder characterized by premature closure of cranial sutures, midfacial hypoplasia and orbital defects. Herein we report a case of this rare entity who presented with brachycephaly, maxillary hypoplasia, wide parrot bea...

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Autors principals: Kaur, Harroop, Singh Waraich, Harmeet, Sharma, Chander Mohan
Format: Artigo
Idioma:Inglês
Publicat: Springer India 2006
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3450369/
https://ncbi.nlm.nih.gov/pubmed/23120355
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/BF03049602
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