@article{shivaswamy2014report,
  title = {Report of Two Cases of Zinsser-Cole-Engman (Dyskeratosis Congenita) Syndrome- A Rare Entity},
  author = {Kanakapura Nanjundaswamy Shivaswamy and A L Shyamprasad and T K Sumathy and C Ranganathan and Praveen Kumar S },
  year = 2014,
  url = {https://ibimapublishing.com/articles/JMED/2014/757802/},
  journal = {JMED Research},
  volume = 2014 (2014),
  pages = 5,
  doi = 10.5171/2014.757802,
  abstract = {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 dyskeratosis congenita of which the first case presented with asymptomatic skin lesions and the second with avascular necrosis of the hip. },
  keywords = {Dyskeratosis, pigmentation, atrophy, leukokeratosis, nail dystrophy.},
  note = Article ID: 757802
}