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May 16, 2011 · Fragile foal syndrome (FFS) type I, formerly known as Warmblood fragile foal syndrome (WFFS) type I, is a recessive inherited connective ...
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Foals with WFFS are naturally aborted, stillborn, or euthanized. WFFS is a genetic defect of connective tissue and foals born with it have hyper-extendible, ...
The syndrome is characterised by soft tissue abnormalities that display in the form of extremely fragile and friable skin, lax and hyper-extensible limb joints, ...
The Warmblood Fragile Foal Syndrome is a hereditary disorder that has been recognized in the United States for several years. A foal with WFFS can be ...
WFFS has been around for more than 170 years. It is caused by a gene mutation that impairs a normal enzyme function critical for the biosynthesis of collagen.
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Warmblood Fragile Foal Syndrome (WFFS) is an inherited autosomal disorder caused by a single mutation in PLOD1 gene. The PLOD1 gene codes for an enzyme that ...
Oct 18, 2021 · Warmblood Fragile Foal Syndrome (WFFS) is an autosomal recessive disorder caused by a mutation in the procollagen-lysine, 2-oxoglutarate ...
Warmblood Fragile Foal Syndrome (WFFS) is a connective tissue disorder in warmbloods that leads to skin detachment. Mutation in the PLOD1 gene.
Dec 5, 2023 · Warmblood Fragile Foal Syndrome (WFFS) is an inherited disease primarily affecting Warmblood horses and their related breeds.