The purpose of the study is to genotype the fibrillin 15 gene in family members and determine whether the mutation segregates with ectopia lentis and/or retinal tear. Through a full Marfan clinical evaluation, we will determine whether isolated ectopia lentis and retinal tear pathology (as compared to the full Marfan syndrome) is associated with this specific mutation in fibrillin 15. Although there is no treatment arm to this research protocol, preventive and palliative therapy will benefit subjects found to have ocular, cardiac or skeletal pathology through clinical services.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000039-41
Application #
6418389
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
1974-10-01
Project End
2004-11-30
Budget Start
Budget End
Support Year
41
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Emory University
Department
Type
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
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