Apert's Syndrome: Ophthalmic Importance and Clinical Findings
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Tarih
2009
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Amer Soc Contemporary Medicine Surgery & Ophthalmology
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Apert's syndrome is a rare form of craniosynostosis that exhibits with many ocular manifestations. We present two cases of Apert's syndrome. Our first case is a 10-year-old girl admitted with exotropia, V pattern and proptosis on examination. Investigations revealed coronal craniosynostosis, cleft palate, vaginal atresia and syndactyly of the hands and feet. The second case is a 5-year-old boy presented with hypertelorism, exotropia, dissociated vertical deviation and proptosis. Investigations revealed coronal craniosynostosis, bifid uvula and syndactyly of the hands and feet
Açıklama
Anahtar Kelimeler
[No Keyword]
Kaynak
Annals of Ophthalmology
WoS Q Değeri
Q4
Scopus Q Değeri
Cilt
41
Sayı
1
