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      • To get a miniature schnauzer DNA tested for myotonia congenita, you just need to arrange a consult with your local vet, so that they can take a blood sample or cheek swab from your dog. This is then sent off to an approved laboratory for testing, which will then return the result of the dog’s status to their owner.
  1. Mar 9, 2023 · Myotonia congenital (schnauzer type) is an inherited muscle disorder affecting miniature schnauzers. The muscle cells of an affected dog are over-excitable, which causes muscles to remain...

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  2. Jan 10, 2024 · Myotonia Congenita (CLCN1 Exon 7, Miniature Schnauzer Variant) This condition is characterized by prolonged muscle contraction and stiffness that usually resolves with normal exercise. The gene is CLCN1 (Exon 7).

  3. Testing Tips. Genetic testing of the CLCN1 gene in miniature schnauzers will reliably determine whether a dog is a genetic Carrier of myotonia congenita (schnauzer type).

  4. Feb 9, 2015 · Paw Print Genetics offers testing for MC and two other diseases reported in the miniature schnauzer. If you’d like to learn more about how you can eliminate MC from your kennel blood line or would like to discuss genetic testing of your dog, feel free to email us at AskUs@pawprintgenetics.com or give us a call at 509-483-5950 to talk to one ...

  5. Objective—To develop a molecular genetic test to detect the mutant skeletal muscle chloride channel (ClC-1) allele that causes myotonia congenita in Miniature Schnauzers and to analyze the relationship of affected and carrier dogs. Animals—372 Miniature Schnauzers from the United States, Canada, Australia, and Europe that were test-

  6. Mar 21, 2022 · To find out the status of a miniature schnauzer when it comes to myotonia congenita, you need to have the dog DNA tested. If you intend to use this information as the basis of planning a mating match, the other dog in the match must be tested too.

  7. www.vet.upenn.edu › genetic-tests › DetailPenn Vet | Genetic Tests

    Heterozygous Carriers (1-2) are not expected to develop signs of Myotonia Congenita but each of their offspring has a chance of inheriting a disease variant allele. Parents, offspring and relatives should also be tested. 1 = Normal allele; 2 = Variant allele.

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