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Crouzon syndrome - A rare case report

Crouzon syndrome is the most common syndrome among the craniosynostosis group. Crouzon syndrome accounts for about 4.8% of all of them. It commonly has autosomal dominant inheritance with complete penetrance and variable expressivity from subtle to severe forms and characterized by craniosynostosis,...

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Dades bibliogràfiques
Publicat a:Int J Health Sci (Qassim)
Autors principals: Kalanjiam, Vidhya, Manoharan, G. V. Murali Gopika
Format: Artigo
Idioma:Inglês
Publicat: Qassim Uninversity 2017
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5654191/
https://ncbi.nlm.nih.gov/pubmed/29085273
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