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Persistent Müllerian Duct Syndrome (PMDS) is a reproductive disorder in which the uterus and other parts of the female reproductive tract develop in male dogs. An important consequence of this disease is cryptorchidism (undescended testicles), which occurs in ~50% of affected dogs and causes infertility, as well as increased risk for testicular tumors. The external genitalia can be otherwise normal, making it easy to overlook PMDS as the underlying cause of cryptorchidism. Female dogs are not affected by this disease.
Note: Cryptorchidism has many potential causes, of which PMDS is only one.
Breeds reported to have Persistent Müllerian Duct Syndrome
The genetic mutation that causes PMDS has been reported in miniature schnauzer dogs, and the test that we offer specifically checks for this mutation. We believe that the mutation is relatively common in this breed (~25% carrier rate, ~2% genetically affected). Mutation screening has not been reported in other breeds. However, PMDS has been described in the papillon, Belgian Malinois, Leonberger, Doberman pinscher, basset hound, and English cocker spaniel. It is unknown if these breeds have the same mutation that causes the disorder in miniature schnauzers or if there are distinct mutations present.
Submitting a sample
Step 1 - Select instructions for your sample type
- Blood sample protocol (pdf)
- Cheek swab protocol (pdf)
- Dew claw & tail docking protocol (pdf)
- Semen sample protocol (pdf)
Step 2 - Complete your submission form(s)
Step 3 - Fees & Payment
- 1-3 dogs - $65 each
- 4 or more - $58 each
Need cheek swabs?
Cheek swabs are not included in the purchase price. Links to several purchasing options are available within the cheek swab protocol (pdf).
Step 4 - Ship your sample(s)
Result interpretation
Scientific references
- Prevalence of the AMHR2 mutation in Miniature Schnauzers and genetic investigation of a Belgian Malinois with persistent Müllerian duct syndrome.
Smit MM, Ekenstedt KJ, Minor KM, Lim CK, Leegwater P, Furrow E.
Reprod Domest Anim. 2017;53(2):371–376. doi: 10.1111/rda.13116 - A single base pair mutation encoding a premature stop codon in the MIS type II receptor is responsible for canine persistent Müllerian duct syndrome.
Wu, X., Wan S., Pujar, S., et al.
J Androl, 2009;30:46-56.