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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...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Kaur, Harroop, Singh Waraich, Harmeet, Sharma, Chander Mohan
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Springer India 2006
Aiheet:
Linkit: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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