Cochlear implantation in a child with subtelomeric 1q deletion syndrome and Dandy-Walker malformation
![Thumbnail](/xmlui/bitstream/handle/20.500.12511/2824/Cevizci-Rasit%202016.pdf.jpg?sequence=5&isAllowed=y)
Göster/ Aç
Erişim
info:eu-repo/semantics/embargoedAccessTarih
2016Yazar
Cevizci, RaşitBezgin Üstün, Selin
Dizdar Turan, Handan
Yılmaz, Oğuz
Kersin, Burak
Bayazıt, Yıldırım Ahmet
Üst veri
Tüm öğe kaydını gösterKünye
Cevizci, R., Bezgin Üstün, S., Dizdar Turan, H., Yılmaz, O., Kersin, B. ve Bayazıt, Y. (2016). Cochlear implantation in a child with subtelomeric 1q deletion syndrome and Dandy-Walker malformation. International Journal Of Pediatric Otorhinolaryngology Extra, 13, 13-15. https://dx.doi.org/10.1016/j.pedex.2016.02.004Özet
Subtelomeric 1q deletion syndrome is a rare disorder characterized by severe mental and growth retardation, microcephaly, distinct facial features and corpus callosum abnormalities. Senserineural hearing loss is not common in this syndrome. We report a 2-year-old boy with subtelomeric 1q deletion syndrome presented with typical craniofacial abnormalities and bilateral senserineural hearing loss. Imaging revealed corpus callosum hypogenesis and Dandy-Walker malformation. Cochlear implantation was successfully undertaken using a transmastoid facial recess aproach. After 12-months post-implantation, good audiological outcomes were obtained. Cochlear implantation can be considered for hearing rehabilitation in patients with subtelomeric 1q deletion syndrome and Dandy-Walker malformation.
Scopus Q Kategorisi
Q4Kaynak
International Journal Of Pediatric Otorhinolaryngology ExtraCilt
13Koleksiyonlar
- Makale Koleksiyonu [3790]
- Makale Koleksiyonu [46]
- Scopus İndeksli Yayınlar Koleksiyonu [6601]
- WoS İndeksli Yayınlar Koleksiyonu [6677]