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- W2007237473 abstract "Apert syndrome is a developmental malformation characterized by craniosynostosis, a cone shaped calvarium, midface hypoplasia, pharyngeal attenuation, ocular manifestations and syndactyly of the hands and feet. The complex craniofacial and systemic deformities seen in Apert syndrome mandate a multidisciplinary approach to improve the quality of life of patients. This paper presents the case of a 27-year-old male patient who presented with the complaints of malaligned teeth, difficulty in chewing food, facial deformity along with syndactyly of the hands and toes, and was diagnosed as a case of Apert syndrome." @default.
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- W2007237473 date "2014-01-01" @default.
- W2007237473 modified "2023-09-24" @default.
- W2007237473 title "Apert syndrome: A rare anomalad" @default.
- W2007237473 doi "https://doi.org/10.4103/2348-3334.138909" @default.
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