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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Principais autores:	Prajakta C Khelkar, Aaditi N Kadam, Freny R Karjodkar, Kaustubh P Sansare
格式:	Artigo
語言:	Inglês
出版:	Wolters Kluwer Medknow Publications 2020-01-01
叢編:	Journal of Indian Society of Pedodontics and Preventive Dentistry
主題:	acrocephalosyndactyly apert's syndrome craniosynostosis exophthalmos hypertelorism micrognathia
在線閱讀:	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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