Konjenital herediter endotelyal distrofide göz bulguları
Küçük Resim Yok
Tarih
1999
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Konjenital herediter endotelyal distrofi (KHED) nadir görülen, otozomal resesif veya otozomal dominant geçiş gösteren bir kornea hastalığıdır. Bu çalışmada KHED'li üç kardeşte (2 kız , 1 erkek) saptanan klinik bulgular sunulmuş, olgularımızda hastalığın klasik bulgularına eşlik eden alternan esotropya ve göziçi basıncı yüksekliği literatür verileri ışığında tartışılmıştır.
Congenital hereditary endothelial dystrophy (CHED) is a rare corneal disorder which is inherited either as an autosomal dominant or autosomal recessive trait. In this article clinical findings in three patients from the same mother (2 sisters , 1 brother) with CHED is presented, alternating esotropia and elevated intraocular pressure accompanying the classic findings of congenital hereditary endothelial dystrophy was discussed under the light of the current literature.
Congenital hereditary endothelial dystrophy (CHED) is a rare corneal disorder which is inherited either as an autosomal dominant or autosomal recessive trait. In this article clinical findings in three patients from the same mother (2 sisters , 1 brother) with CHED is presented, alternating esotropia and elevated intraocular pressure accompanying the classic findings of congenital hereditary endothelial dystrophy was discussed under the light of the current literature.
Açıklama
Anahtar Kelimeler
Göz Hastalıkları
Kaynak
Türkiye Klinikleri Oftalmoloji Dergisi
WoS Q Değeri
Scopus Q Değeri
Cilt
8
Sayı
2
