Meeting Banner
Abstract #3437

Different genetic mutations are associated with different abnormal patterns of language white matter pathways in young children with global developmental delay

JEONG-WON JEONG 1 , Senthil Sundaram 1 , Diane C. Chugani 1 , and Harry T. Chugani 1

1 Pediatrics and Neurology, Wayne State University, Detroit, Michigan, United States

Global developmental delay (GD) refers to an etiologically heterogeneous set of neurodevelopmental disorders mediated in part by multiple genetic mutations. The present study investigates whether a "maximum a posteriori probability (MAP)" classifier, a diffusion weighted imaging (DWI) tractography method, can be used to detect unique patterns in axonal language pathways, which may be correlated to different types of genetic mutations observed in children with GD.

How to access this content:

For one year after publication, abstracts and videos are only open to registrants of this annual meeting. Registrants should use their existing login information. Non-registrant access can be purchased via the ISMRM E-Library.

After one year, current ISMRM & ISMRT members get free access to both the abstracts and videos. Non-members and non-registrants must purchase access via the ISMRM E-Library.

After two years, the meeting proceedings (abstracts) are opened to the public and require no login information. Videos remain behind password for access by members, registrants and E-Library customers.

Click here for more information on becoming a member.

Keywords