Apert's Syndrome: Ophthalmic Importance and Clinical Findings

[ X ]

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

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Kaynak

Annals of Ophthalmology

WoS Q Değeri

Q4

Scopus Q Değeri

Cilt

41

Sayı

1

Künye