Apert's syndrome: A rare craniofacial disorder
Apert's syndrome (AS) which is a rare congenital disorder is a form of acrocephalosyndactyly. This syndrome is characterized by craniosynostosis, midface hypoplasia, and syndactyly of hands and feet. We report a case of 13-year-old boy in India presenting features of AS such as exophthalmos, hyperte...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Wolters Kluwer Medknow Publications
2020-01-01
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| Edice: | Journal of Indian Society of Pedodontics and Preventive Dentistry |
| Témata: | |
| On-line přístup: | http://www.jisppd.com/article.asp?issn=0970-4388;year=2020;volume=38;issue=4;spage=430;epage=433;aulast=Khelkar |
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