Punctal and Canalicular Obstruction Associated with Dyskeratosis Congenita
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Case Report
VOLUME: 45 ISSUE: 1
P: 40 - 41
January 2015

Punctal and Canalicular Obstruction Associated with Dyskeratosis Congenita

Turk J Ophthalmol 2015;45(1):40-41
1. Gülhane Askeri Tip Akademisi Haydarpasa Egitim Hastanesi, Göz Hastaliklari Klinigi, Istanbul, Türkiye\R\N
2. Gülhane Askeri Tip Akademisi Haydarpasa Egitim Hastanesi, Göz Hastaliklari Klinigi, Istanbul, Türkiye
3. Gülhane Askeri Tip Akademisi Haydarpasa Egitim Hastanesi, Cildiye Klinigi, Istanbul, Türkiye
No information available.
No information available
Received Date: 24.01.2014
Accepted Date: 15.04.2014
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ABSTRACT

Dyskeratosis congenita is a rare X-linked recessive, multisystem disease characterized by bone marrow failure, oral leukoplakia, nail dystrophy, and reticular skin pigmentations. It is also associated with ocular abnormalities. In this article, we present a young male with a diagnosis of dyskeratosis congenita who had reticulated hyperpigmented skin lesions on the neck, shoulders and upper eyelids, bilateral punctal and canalicular obstruction, and dystrophic nails.

Keywords:
Dyskeratosis congenita, punctal and canalicular obstruction