[Oral findings in dyskeratosis congenita (a case report)]

Autor: A, Parlar, T, Oygür, O, Demir, O, Gazioğlu
Rok vydání: 1989
Předmět:
Zdroj: Ankara Universitesi Dis Hekimligi Fakultesi dergisi = The Journal of the Dental Faculty of Ankara University. 16(1)
ISSN: 1016-8710
Popis: 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.
Databáze: OpenAIRE