Summary of Purpose
Fabry's disease a genetic disorder (X-linked recessive) due to the absence of the enzyme alpha-galactosidase A. The disease is characterized by abnormal collections of glycolipids in cells (histiocytes) within blood vessel walls, tumors on the thighs, buttocks, and genitalia, decreased sweating, tingling sensations in the extremities, and cataracts. Patients with Fabry 's disease die from complications of the...Read More →
The following dates are available for this trial. Trial information last updated on 3 March 2008.
|1 Oct 1997||3 Nov 1999||Unavailable||1 Oct 2000||1 Nov 1999||Unavailable|
|Start Date||First Received||1st Completion||Completion||Verification||Results|