| Literature DB >> 2637028 |
A Parlar, T Oygür, O Demir, O Gazioğlu.
Abstract
Dyskeratosis congenita is a rare genokeratosis and characterized by, A) Reticular dermal atrophy and telangiectatic pigmentation, B) Distrophies of the nails, C) Oral leukokeratosis. In this article, a 22 year old male patient with Dyskeratosis congenita was presented and oral findings were discussed.Entities:
Mesh:
Year: 1989 PMID: 2637028
Source DB: PubMed Journal: Ankara Univ Hekim Fak Derg ISSN: 1016-8710