Inherited patterned lentiginosis is an inherited skin condition that results in widespread small, flat areas of more-pigmented skin with clearly defined borders, generally noticed when the affected person is an infant or young child.[1] The inheritance pattern is autosomal dominant,[2]: 686 and organs other than the skin are not affected; therefore, it is distinct from Carney complex.[1][3]
| Inherited patterned lentiginosis | |
|---|---|
| Other names | Familial lentigines profusa |
 | |
| Autosomal dominant is the inheritance manner of this condition | |
| Specialty | Dermatology |
References
edit- ^ a b Online Mendelian Inheritance in Man (OMIM): Inherited Patterned Lentiginosis - 151001
- ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
- ^ Xing, Qinghe; Chen, Xiangdong; Wang, Mingtai; Bai, Wenjie; Peng, Xin; Gao, Rui; Wu, Shengnan; Qian, Xueqing; Qin, Wei (July 2005). "A locus for familial generalized lentiginosis without systemic involvement maps to chromosome 4q21.1-q22.3". Human Genetics. 117 (2–3): 154–159. doi:10.1007/s00439-005-1284-1. ISSN 0340-6717. PMID 15841387.