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Apert syndrome: A case report

European Journal of Dentistry · Ocak 2012

Makale Bilgileri

DergiEuropean Journal of Dentistry
Yayın TarihiOcak 2012
Cilt / Sayfa6 · 110-113
Erişim🔓 Açık Erişim
Özet The purpose of this report is to present Apert syndrome patient by highlighting craniofacial characteristics and orthodontic approach to treatment. The patient, a 16-day-old female and the second child of healthy parents, was admitted to our department with primary complaint of cleft palate. She had a cone-shaped calvarium, midface hypoplasia, syndactyly of the hands and feet, hypertelorism, proptosis and cleft palate. After taking maxillary impression, an acrylic appliance was applied to orientate the growing and enable the feeding. A case with Apert syndrome undergoes the orthodontic treatment for a long time and also a multidisciplinary approach is essential to determine the best collaborative corrective plan for the deficiencies of the patient.

Yazarlar (2)

1
Zehra Ileri
2
Yasar Bedii Goyenc

Anahtar Kelimeler

Apert syndrome Craniosynostosis Newborn infant

Kurumlar

Private Practice
Balikesir Turkey
Selçuk Üniversitesi
Selçuklu Turkey

Metrikler

5
Atıf
2
Yazar
3
Anahtar Kelime

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