Jackson-Weiss syndrome

Your Results

Sign In

Description

Jackson-Weiss syndrome (JWS) is an autosomal dominant condition consisting of craniosynostosis characterized by premature fusion of the cranial sutures as well as radiographic anomalies of the feet (summary by Heike et al., 2001).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

External Links

© 2024 Biocodify. All rights reserved.

Stay up to date

The latest news and updates from Biocodify, sent to your inbox.