Clinical Characterization of Inherited Patterned Lentiginosis
-
- STATUS
- None
Summary
Inherited lentigines syndromes are characterized by multiple small, light to very dark brown or black evenly pigmented macules. Several of these syndromes are associated with systemic abnormalities including predisposition to internal malignancy. Inherited Patterned Lentiginosis is an autosomal dominant syndrome for which the genetic mutation(s) have yet to be elucidated. This observational case-series will carefully describe the clinical phenotype of Inherited Patterned Lentiginosis. Additionally, this study will investigate the genetic mutation(s) associated with IPL through genotyping of DNA obtained from saliva samples from affected and non-affected family members.
Details
| Condition | TBD, tbd, tbd |
|---|---|
| Age | 99years or below |
| Clinical Study Identifier | TBD |
| Last Modified on | 19 February 2024 |
Similar trials to consider
Not finding what you're looking for?
Sign up as a volunteer to stay informed
Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.
Sign up as volunteerStudy Definition
WikipediaAdd a private note
- Select a piece of text.
- Add notes visible only to you.
- Send it to people through a passcode protected link.