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Dual-mode Imaging of Cutaneous Tissue Oxygenation and Vascular Function
Published on: December 8, 2010
Dyskeratosis congenita: presentation of cutaneous triad in a sporadic case
Reena Kumari Sharma1, Mudita Gupta1, Samriti Sood1
1Department of Dermatology, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India.
Abstract:
Dyskeratosis congenita (DKC) also known as Zinsser-Cole-Engman syndrome is a progressive genetic disease with a classical presentation characterised by a triad of reticulate pigmentation of skin, nail dystrophy and leukoplakia. It may be a multisystem disease with the involvement of haematological, gastrointestinal, genitourinary, neurological, ophthalmic, pulmonary and skeletal system. We report a sporadic case of DKC presenting with poikiloderma, nail dystrophy and oral leukoplakia.
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