LABOKLIN Service ID: 8538<\/span><\/p> TaqMan SNP assay (Miniature Schnauzer); Lancashire Heeler, Miniature Schnauzer<\/p><\/td><\/tr> autosomal recessive<\/p><\/td><\/tr> 3 - 5 days after arrival of the sample in the lab (Miniature Schnauzer); Charcot-Marie-Tooth neuropathy (CMT)LABOKLIN Service ID: 8538Charcot-Marie-Tooth neuropathy (CMT) is a heterogeneous group of inherited peripheral neuropathies affecting the peripheral sensory and motor nerves. CMT is the most common neuromuscular disorder in humans.In the breed Miniature Schnauzer, a variant in the SBF2 gene (also known as MTMR13 gene) has been found to cause Charcot-Marie-Tooth neuropathy (CMT).…<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":1419953,"menu_order":7,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_seopress_robots_primary_cat":"","_seopress_titles_title":"","_seopress_titles_desc":"","_seopress_robots_index":"","footnotes":""},"class_list":["post-1426542","page","type-page","status-publish","hentry","description-off"],"_links":{"self":[{"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/pages\/1426542","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/comments?post=1426542"}],"version-history":[{"count":0,"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/pages\/1426542\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/pages\/1419953"}],"wp:attachment":[{"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/media?parent=1426542"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Charcot-Marie-Tooth neuropathy (CMT)<\/strong> is a heterogeneous group of inherited peripheral neuropathies<\/strong> affecting the peripheral sensory and motor nerves. CMT is the most common neuromuscular disorder in humans.
In the breed Miniature Schnauzer<\/strong>, a variant in the SBF2 gene (also known as MTMR13 gene) has been found to cause Charcot-Marie-Tooth neuropathy (CMT). Affected dogs show regurgitations caused by mega-esophagus and inspiratory dyspnea caused by laryngeal paralysis<\/strong> at a young age (< 2 years). In the previously described cases, affected dogs have been alive more than 3 years following diagnosis which indicates a long survival rate. Typical pathological findings are variable thickness of the myelin sheath (so-called \u201ctomacula\u201d) around the axons of peripheral nerves and areas of segmental demyelination. The described variant has not been found in other breeds than Miniature Schnauzers.
In the breed Lancashire Heeler<\/strong>, a genetic variant of the ITPR3 gene has been found to be associated with CMT. Due to a severe developmental enamel defect, affected dogs show features of amelogenesis imperfecta, including severe yellow to brown discoloration, enamel hypoplasia and abrasion leading to dentin exposure<\/strong>. The second common symptom of the disease is a subclinical peripheral neuropathy<\/strong>. Therefore, affected dogs show normal locomotion and activity levels, but electrodiagnostic examinations emerge neurogenic changes in muscle, especially in muscles distal to elbow and knee joints, consistent with demyelinating neuropathy.<\/p>Method<\/strong><\/td>
sequencing (Lancashire Heeler)<\/p><\/td><\/tr>Breed list<\/strong><\/td> Heredity<\/strong><\/td> Duration<\/strong><\/td>
1 - 2 weeks after arrival of the sample in the lab (Lancashire Heeler)<\/p><\/td><\/tr><\/table>\n","protected":false},"excerpt":{"rendered":"