HAX1 Sequencing

Test Background

Mutations in HAX1 result in severe congenital neutropenia/Kostmann disease, which are disorders of hematopoiesis. There are several types. This particular type is inherited in an autosomal recessive manner.

This laboratory performs Sanger sequencing of the HAX1 gene.

Gene(s)

HAX1

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.