Inherited patterned lentiginosis
Medical condition From Wikipedia, the free encyclopedia
Medical condition From Wikipedia, the free encyclopedia
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 |
Seamless Wikipedia browsing. On steroids.
Every time you click a link to Wikipedia, Wiktionary or Wikiquote in your browser's search results, it will show the modern Wikiwand interface.
Wikiwand extension is a five stars, simple, with minimum permission required to keep your browsing private, safe and transparent.
