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Binders syndrome an unusual craniofacial anomaly

Nomor Panggil J-pdf 25:1 (2018)
Pengarang lain/Kontributor
Penerbitan Jakarta: Journal of Dentistry Indonesia, 2018
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Sumber PengataloganLibUI engind rda
PertanggungjawabanAnanya Madiyal, Subhas Babu, Vidya Ajila, Renita Lorina Castelino, Kumuda Rao, Medhini Madi
Majalah/JurnalJournal of Dentistry Indonesia
VolumeVol. 25, No. 1, April 2018: 69-72
Tipe Konten text
Tipe Media computer
Tipe Carrier online resource
Akses Elektronik
Institusi Pemilik Universitas Indonesia
Lokasi Perpustakaan UI, Lantai 4, R. Koleksi Jurnal
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J-pdf 25:1 (2018) 03-19-908417313 TERSEDIA
Tidak ada ulasan pada koleksi ini: 20495732
Binders syndrome or maxillonasal dysostosis is a rare congenital condition that primarily affects the mid face and sometimes the vertebrae. It was named after von Binder who described three cases of hypoplastic maxilla nasal complex in 1962. It can either occur as a sporadic mutation or may be inherited in an autosomal recessive pattern with incomplete penetrance. Decrease in the naso labial angle, flat forehead, dish shaped face, absence of protrusion of nasal tip, absence of nasal flare with triangular or semilunar nostrils, palpable depression in the nasal floor and a class III tendency are characteristic of the syndrome. Vertebral anomalies are seen in some patients owing to the parallel development of the nasal complex and vertebrae in the third month of intrauterine life. Prenatal diagnosis may be done using ultrasonography at 21 weeks of pregnancy. A multi disciplinary approach towards planning of treatment for individuals with Binders syndrome includes orthodontic treatment along with osteotomies and grafting to correct the nasal and mid face defects.