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Abant İzzet Baysal Ü. Düzce Tıp Fak. Göz Hast. ABD., Bolu. Tbp.Atğm. Mareşal Çakmak Asker Hastanesi, Göz Hastalıkları Bölümü, Erzurum Primary persistant hyperplastic vitreous associating with morning glory syndrome was diagnosed in a 22 year-old male admitted to our clinic for a low vision complaint on his left eye since early childhood. Co-existance of these two developmental disorders suggest a failure in a common embryogenic step. The clinical characteristics of this very rare condition should be considered in differantial diagnosis and treatment. Keywords : Morning glory syndrome, primary persistant hyperplastic vitreous