Dr. van Haeringen Laboratorium B.V.

P318 Warmblood Fragile Foal Syndrome (WFFS)


Warmblood Fragile Foal Syndrome (WFFS) is a hereditary disease with symptoms of hyperextensible and abnormally fragile skin, as well as hyperextensibility of articulations. The skin of newborn foals lacks tensile strength due to large spaces between deep dermal fibers. Also, lesions occur across the body and limb joints are extremely lax and hyperextensible. These abnormalities require euthanasia just after delivery. The defect is caused by a point mutation on the PLOD1 gene, which results in an incomplete protein folding (c.2032G>A, p.Gly678Arg).

Test specific information

The test for detecting WFFS is patented in Germany, France and Great Britain, only. For this test, we cooperate with our sisterlab, VHL in Wageningen to which we forward the anonymized sample material for testing.


Symptoms will develop at a young age. Within a few hours to a maximum of several weeks after birth, the characteristics that go with these genetic effects will become visible.

Turnaround time

The Turnaround Time (TAT) depends on various factors, such as the shipment time of your sample to the test location, the test method(s) and whether the tests are performed completely or partially by a Partner Lab or Patent owner.

The TAT of tests performed at our facilities is normally 10 working days after receipt of the sample at the testing laboratory (VHL, VHP or Certagen). For tests performed by a Partner Laboratory (so-called "partner lab test") or patent owner, the TAT is at least 20 working days after receipt of your sample. Because the shipment time to our Partner Labs or patent owner may vary due to factors we cannot influence, the mentioned 20 working days are therefore an estimate.

Sometimes it is necessary to re-run your sample. We call this a retest. In that case, the TAT will of course be extended.

Location of disease or trait

Trait or disease of coat or skin.

Breed dependence

This DNA test is available for the following breeds: Warmblood. Additional information is available in the Frequently Asked Questions (FAQ).

Sample type

For this DNA test we accept the following materials: Blood EDTA, Blood Heparin, Semen, Hair. Please contact Dr. Van Haeringen Laboratorium if you wish to submit other material as listed.


An animal can be free and has in that situation two healthy alleles. When used in breeding this animal will not become ill due to the disease. It cannot spread the disease in the population.

An animal can be carrier and has in that situation one healthy and one disease allele. When used in breeding 50 percent of the offspring will receive the disease allele. Carriers will not become ill.

An animal can be affected and has in that situation two disease alleles. When used in breeding all offspring will also receive the disease allele. Affected will become ill.


This genetic factor is inherited in an autosomal, recessive, mode. This means, that the individual can be free of the disease (homozygote normal), affected (homozygous affected) or carrier (heterozygous).

Carriers may spread the mutation in a population without showing symptoms themselves. Because of this, it is extremely important to identify carriers correctly to prevent spreading of a mutation.

Severity of Disease

Disease with severe symptoms, which additionally may rapidly progress, as well as lethal diseases.

Code P318

Warmblood Fragile Foal Syndrome (WFFS)

€ 57,48 (Incl. 21% VAT)
€ 47,50 (Excl. VAT)