Reticular pigmented anomaly of the flexures
From Wikipedia, the free encyclopedia
Medical condition
| Reticular pigmented anomaly of the flexures | |
|---|---|
| Other names | Kitamura reticulate acropigmentation[1] |
| Specialty | Dermatology |
Reticular pigmented anomaly of the flexures (also known as dark dot disease and Dowling–Degos disease) is a fibrous anomaly of the flexures or bending parts of the axillae, neck and inframammary/sternal areas.[2] : 856 It is an autosomal-dominant pigmentary disorder that may appear in adolescence or adulthood. This condition is due to mutations in structural/desmosomal proteins found within stratified squamous epithelium.[3]
Dark dot disease is associated with KRT5 .[4]
See also
[edit ]- List of cutaneous conditions
- List of cutaneous conditions caused by mutations in keratins
- Skin lesion
References
[edit ]- ^ "Dowling-Degos disease | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on April 23, 2019. Retrieved 23 April 2019.
- ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
- ^ Betz RC, Planko L, Eigelshoven S, et al. (March 2006). "Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease". Am. J. Hum. Genet. 78 (3): 510–9. doi:10.1086/500850. PMC 1380294 . PMID 16465624.
External links
[edit ]
