Dyskeratosis
Medical condition
Medical condition
| Dyskeratosis | |
|---|---|
| Specialty | Dermatology |
Dyskeratosis is abnormal keratinization occurring prematurely within individual cells or groups of cells below the stratum granulosum.[1]
Dyskeratosis congenita is congenital disease characterized by reticular skin pigmentation, nail degeneration, and leukoplakia on the mucous membranes associated with short telomeres.[2]
See also
- Skin lesion
- Skin disease
- List of skin diseases
References
- ^ Kumar, Vinay; Fausto, Nelso; Abbas, Abul (2004) Robbins & Cotran Pathologic Basis of Disease (8th ed.). Saunders. Page 1392. ISBN 0-7216-0187-1.
- ^ Mason PJ, Bessler M (2011). "The genetics of dyskeratosis congenita". Cancer Genetics. 204 (12): 635–645. doi:10.1016/j.cancergen.2011.11.002. PMC 3269008. PMID 22285015.
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Skin lesion terminology
| Primary lesions |
|
|---|---|
| Secondary lesions |
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- keratin: Hyperkeratosis
- Parakeratosis
- Dyskeratosis
- Hypergranulosis
- Acanthosis
- Papillomatosis
- Acantholysis
- Spongiosis
- Hydropic swelling
- Exocytosis
- Vacuolization
- Erosion
- Ulceration
- Lentiginous
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