Report of Two Cases of Zinsser-Cole-Engman (Dyskeratosis Congenita) Syndrome- A Rare Entity
JMED Research
Zinsser-Cole-Engman syndrome, also known as dyskeratosis congenita, is a rare genetic disorder characterized by triad of pigmentation and atrophy of the skin, leukokeratoses of oral mucosa and nail dystrophy along with bone marrow failure and predisposition to cancer. Here, we are reporting two cases of…