Next Generation Sequencing for a Family with Multigenerational Femoroacetabular Impingement

Overview

About this study

The purpose of this study is to determine potential genetic predisposition to FAI through NGS in a family with multigenerational disease. Provide genetic counseling and orthopedic management options to family members with unknown disease status. Establish screening and risk-stratification parameters via NGS through publication of genetic abnormalities associated with FAI.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Members of the family identified with multigenerational FAI.

Exclusion Criteria:

None

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status	Contact
Rochester, Minn. Mayo Clinic principal investigator Rafael Sierra, M.D.	Closed for enrollment	Contact information: Teron Cox CCRP (507) 538-3560 Cox.Teron@mayo.edu

Mayo Clinic Location

Status

Contact

Rochester, Minn.

Mayo Clinic principal investigator

Rafael Sierra, M.D.

Closed for enrollment

Contact information:

Teron Cox CCRP

(507) 538-3560

Cox.Teron@mayo.edu

More information

Publications

Publications are currently not available

Clinical Trials