This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Ehlers-Danlos syndrome (EDS) type IV, also known as the vascular type of EDS, is a rare inherited disorder in which affected individuals have a decreased life expectancy because they are at risk for arterial and bowel rupture. The dominantly inherited disorder results from mutations in the COL3A1 gene that encodes the chains of type III collagen, a component of the walls of blood vessels and bowel. We will take detailed histories, complete detailed physical examinations, assemble complete medical documentation, and image, by high resolution MRI, portions of the vascular tree of individuals with genetically documented mutations in the COL3A1 gene to determine if characteristics of arterial wall could point to specific useful therapies. The GCRC will be used for interviews and exams.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000037-46
Application #
7379367
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2006-04-01
Project End
2007-03-31
Budget Start
2006-04-01
Budget End
2007-03-31
Support Year
46
Fiscal Year
2006
Total Cost
$7,443
Indirect Cost
Name
University of Washington
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
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Han, Seung Jin; Fujimoto, Wilfred Y; Kahn, Steven E et al. (2018) Change in visceral adiposity is an independent predictor of future arterial pulse pressure. J Hypertens 36:299-305

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