Add like
Add dislike
Add to saved papers

CYLD-related cutaneous syndrome : variable p.Pro482fs*6 phenotype in five individuals from two unrelated families.

Familial cylindromatosis has been first reported back to 1842 by Ancell. Brooke-Spiegler syndrome was described in 1892 by Brooke in a British family with multiple trichoepitheliomas and in 1899 by Spiegler in an Austrian individual who had cylindromas. CYLD mutations have been identified in the following distinct entities : familial cylindromatosis (FC) (OMIM: 132700), multiple familial trichoepitheliomas (MFT) (OMIM: 601606) and Brooke-Spiegler syndrome (BSS) (OMIM: 605041). A generic term for these three entities, namely CYLD cutaneous syndrome, has been proposed1.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app