F13B Sequencing

Test Background

Mutations in F13B result in factor XIIIB deficiency, which is characterized by increased bleeding and poor wound healing. This condition is inherited in an autosomal recessive manner.

This laboratory performs Sanger sequencing of the F13B gene.

Gene(s)

F13B

About Claritas

Claritas Genomics serves children affected with complex genetic disorders by providing timely and accurate results, resolving families’ long search for answers. By combining clinical expertise of the world’s best pediatric specialists with innovative platform solutions, Claritas is working to improve patient care and enable new discoveries. We are committed to the highest quality and accessibility of information and our interpretive services and unique approach to reporting set the standard for reliably and clearly communicating genetic information.

Now is the time to integrate genomics into clinical practice to inform, guide and improve medical treatment for kids around the world.