Skip to search formSkip to main contentSkip to account menu

Orofaciodigital Syndrome Type 1

An X-linked inherited syndrome caused by mutations in the OFD1 gene mapped to chromosome Xp22.2. It is characterized by malformations of the face… 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Facial comedonal acne in orofaciodigital syndrome type 1 caused by a novel frameshift variant in OFD1
an underestimate because of the difficulty in detection of motor involvement in specific areas, such as in ophthalmic and… 
2018
2018
Successful treatment of facial milia in an infant with orofaciodigital syndrome type 1
We report the successful treatment of multiple facial milia with manual extraction and tretinoin in a child with orofaciodigital… 
2007
2007
Oro-facio-digital syndrome type 1: imaging findings in an 11-year-old girl.
We describe a uniquely illustrated case of orofaciodigital syndrome type 1. We document many of the possible features of this… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)