Punctal and Canalicular Obstruction Associated with Dyskeratosis Congenita

Dyskeratosis congenita is a rare X-linked recessive, multisystem disease characterized by bone marrow failure, oral leukoplakia, nail\uddystrophy, and reticular skin pigmentations. It is also associated with ocular abnormalities. In this article, we present a young male with\uda diagnosis of dyskeratosis congenita who had reticulated hyperpigmented skin lesions on the neck, shoulders and upper eyelids, bilateral\udpunctal and canalicular obstruction, and dystrophic nails. (Turk J Ophthalmol 2015; 45: 40-41