| Literature DB >> 23060386 |
Neelisha Pandey1, Ramesh Kumar Pandey, Rajeev Kumar Singh, Naveen Kumar Shah.
Abstract
Crouzon syndrome is a rare genetic disorder caused due to genetic mutations. It is characterised by partial hearing loss, dry eyes, strabismus and underdevelopment of the upper jaw with facial deformities and malocclusion. These facial deformities greatly affect the social and emotional development of the affected child. The present case report highlights the social problems faced by a child suffering with Crouzon syndrome.Entities:
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Year: 2012 PMID: 23060386 PMCID: PMC4544844 DOI: 10.1136/bcr-2012-007242
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X