{"id":248206,"date":"2024-09-12T07:23:56","date_gmt":"2024-09-12T05:23:56","guid":{"rendered":"http:\/\/staging.laboklin.com\/labogen\/labogen_wp\/congenital-myasthenic-syndrome-cms"},"modified":"2024-09-12T07:23:56","modified_gmt":"2024-09-12T05:23:56","slug":"congenital-myasthenic-syndrome-cms","status":"publish","type":"page","link":"https:\/\/labogen.com\/en\/genetic-diseases-dog\/congenital-myasthenic-syndrome-cms\/","title":{"rendered":"Congenital myasthenic syndrome (CMS)"},"content":{"rendered":"<div class=\"wrap-top\"><div class=\"wrap-left\"><h1 class=\"header-1\">Congenital myasthenic syndrome (CMS)<\/h1><h4><strong>General description<\/strong><\/h4><p class=\"bodytext\">Symptoms of the disease are most of all a generalized skeletal muscle weakness, which worsens especially after exercise, stress or excitement. Signs can already be seen at just two weeks of age. Mobility and spinal reflexes of all limbs are reduced.<\/p><h4 class=\"header-4\"><strong><span>Breeds<\/span><\/strong><\/h4><p>Australian-Labradoodle (Cobberdog), Golden Retriever, Goldendoodle, Heideterrier, Jack Russell Terrier, Labradoodle, Labrador Retriever, Old Danish Pointing Dog, Parson Russell Terrier<\/p><div class=\"wrap-detailed\"><details><summary class=\"detail-summary\">Detailed description<\/summary><p class=\"detailed\"><p><strong>Congenital myasthenic syndrome (CMS)<\/strong> is a inherited <strong>neuromuscular disorder<\/strong> in dogs. It leads to a <strong>generalized muscle weakness<\/strong> that becomes more pronounced after <strong>physical exertion<\/strong>, <strong>stress<\/strong>, or <strong>excitement<\/strong>.<\/p> <p>Affected puppies often show <strong>first symptoms at just a few weeks of age<\/strong> \u2013 in some cases as early as the second week of life. The dogs tire quickly, their movements become unsteady, and they increasingly struggle to support their own body weight.<\/p><\/p><\/details><\/div><\/div><div class=\"clear-both\"><\/div><\/div><div class=\"wrap-top\"><div class=\"wrap-left\"><h4>Congenital myasthenic syndrome (CMS) - Golden Retriever<\/h4><p class=\"bodytext\">The <strong><em>COLQ<\/em> gene<\/strong> is responsible for anchoring the enzyme acetylcholinesterase at the neuromuscular junction. This enzyme breaks down the neurotransmitter acetylcholine after signal transmission. Due to the <em>COLQ<\/em> gene variant, acetylcholine remains active for too long, which <strong>disrupts signal transmission<\/strong> and <strong>overstimulates the muscles<\/strong>. First signs usually appear in Golden Retrievers around the age of <strong>4 weeks<\/strong>.<\/p><\/div><div class=\"wrap-right\"><div class=\"wrap-toggle\"><div class=\"toggle-details\"><details><summary class=\"summary-details\">Order details<\/summary><table border=\"0\"><tr><td width=\"45%\"><span><strong>Test number<\/strong><\/span><\/td><td>8206<\/td><\/tr><tr><td><strong>Sample material<\/strong><\/td><td>0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT)<\/td><\/tr><tr><td><strong>Test duration<\/strong><\/td><td>7-14 working days<\/td><\/tr><\/table><\/details><details><summary class=\"summary-specs\">Test specifications<\/summary><table border=\"0\"><tr><td width=\"45%\"><strong>Symptom complex<\/strong><\/td><td>muscular<\/td><\/tr><tr><td width=\"45%\"><strong>Inheritance<\/strong><\/td><td>autosomal recessive<\/td><\/tr><tr><td width=\"45%\"><strong>Age of onset<\/strong><\/td><td>4 weeks <\/td><\/tr><tr><td width=\"45%\"><strong>Causality<\/strong><\/td><td>causally<\/td><\/tr><tr><td width=\"45%\"><strong>Gene<\/strong><\/td><td>LOC608697<\/td><\/tr><tr><td width=\"45%\"><strong>Mutation<\/strong><\/td><td>G-A<\/td><\/tr><tr><td width=\"45%\"><strong>Literature<\/strong><\/td><td><a href='https:\/\/www.omia.org\/OMIA001928\/9615\/' target='_blank'>OMIA:001928-9615<\/a><\/td><\/tr><\/table><\/details><\/div><div class=\"order-now\"><strong><a href=\"https:\/\/shop.labogen.com\">Order now ...<\/a><\/strong><\/div><\/div><\/div><div class=\"clear-both\"><\/div><\/div><div class=\"wrap-top\"><div class=\"wrap-left\"><h4>Congenital myasthenic syndrome (CMS) - Labrador Retriever<\/h4><p class=\"bodytext\">The <strong><em>COLQ<\/em> gene<\/strong> is responsible for anchoring the enzyme acetylcholinesterase at the neuromuscular junction. This enzyme breaks down the neurotransmitter acetylcholine after signal transmission. Due to the <em>COLQ<\/em> gene variant, acetylcholine remains active for too long, which <strong>disrupts signal transmission<\/strong> and <strong>overstimulates the muscles<\/strong>. First signs usually appear in Labrador Retriever puppies around the age of <strong>6 weeks<\/strong>.<\/p><\/div><div class=\"wrap-right\"><div class=\"wrap-toggle\"><div class=\"toggle-details\"><details><summary class=\"summary-details\">Order details<\/summary><table border=\"0\"><tr><td width=\"45%\"><span><strong>Test number<\/strong><\/span><\/td><td>8206<\/td><\/tr><tr><td><strong>Sample material<\/strong><\/td><td>0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT)<\/td><\/tr><tr><td><strong>Test duration<\/strong><\/td><td>7-14 working days<\/td><\/tr><\/table><\/details><details><summary class=\"summary-specs\">Test specifications<\/summary><table border=\"0\"><tr><td width=\"45%\"><strong>Symptom complex<\/strong><\/td><td>muscular<\/td><\/tr><tr><td width=\"45%\"><strong>Inheritance<\/strong><\/td><td>autosomal recessive<\/td><\/tr><tr><td width=\"45%\"><strong>Age of onset<\/strong><\/td><td>6 weeks <\/td><\/tr><tr><td width=\"45%\"><strong>Causality<\/strong><\/td><td>causally<\/td><\/tr><tr><td width=\"45%\"><strong>Gene<\/strong><\/td><td>LOC608697<\/td><\/tr><tr><td width=\"45%\"><strong>Mutation<\/strong><\/td><td>T-C<\/td><\/tr><tr><td width=\"45%\"><strong>Literature<\/strong><\/td><td><a href='https:\/\/www.omia.org\/OMIA001928\/9615\/' target='_blank'>OMIA:001928-9615<\/a><\/td><\/tr><\/table><\/details><\/div><div class=\"order-now\"><strong><a href=\"https:\/\/shop.labogen.com\">Order now ...<\/a><\/strong><\/div><\/div><\/div><div class=\"clear-both\"><\/div><\/div><div class=\"wrap-top\"><div class=\"wrap-left\"><h4>Congenital myasthenic syndrome (CMS) - Old Danish Pointing Dog<\/h4><p class=\"bodytext\"><p>The <strong><em>CHAT<\/em> gene<\/strong> controls the production of the enzyme choline acetyltransferase, which synthesizes the neurotransmitter acetylcholine in nerve cells. Due to the gene variant, insufficient acetylcholine is produced, leading to a <strong>disturbed transmission of signals from nerve to muscle<\/strong> and thus to <strong>rapid muscle fatigue<\/strong>.<\/p> <p>A typical feature is that the weakness temporarily improves after a short rest, but quickly returns with renewed activity. Thus, affected dogs can initially walk normally for a few minutes, then take shorter and shorter steps and eventually collapse from exhaustion; after a few minutes of rest, they can get up and walk again, before symptoms recur with continued exertion.<\/p> <p>First symptoms may appear as early as <strong>2 weeks of age<\/strong>.<\/p><\/p><\/div><div class=\"wrap-right\"><div class=\"wrap-toggle\"><div class=\"toggle-details\"><details><summary class=\"summary-details\">Order details<\/summary><table border=\"0\"><tr><td width=\"45%\"><span><strong>Test number<\/strong><\/span><\/td><td>8206<\/td><\/tr><tr><td><strong>Sample material<\/strong><\/td><td>0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT)<\/td><\/tr><tr><td><strong>Test duration<\/strong><\/td><td>7-14 working days<\/td><\/tr><\/table><\/details><details><summary class=\"summary-specs\">Test specifications<\/summary><table border=\"0\"><tr><td width=\"45%\"><strong>Symptom complex<\/strong><\/td><td>muscular<\/td><\/tr><tr><td width=\"45%\"><strong>Inheritance<\/strong><\/td><td>autosomal recessive<\/td><\/tr><tr><td width=\"45%\"><strong>Age of onset<\/strong><\/td><td>2 weeks <\/td><\/tr><tr><td width=\"45%\"><strong>Causality<\/strong><\/td><td>causally<\/td><\/tr><tr><td width=\"45%\"><strong>Gene<\/strong><\/td><td>CHAT<\/td><\/tr><tr><td width=\"45%\"><strong>Mutation<\/strong><\/td><td>G-A<\/td><\/tr><tr><td width=\"45%\"><strong>Literature<\/strong><\/td><td><a href='https:\/\/www.omia.org\/OMIA002072\/9615\/' target='_blank'>OMIA:002072-9615<\/a><\/td><\/tr><\/table><\/details><\/div><div class=\"order-now\"><strong><a href=\"https:\/\/shop.labogen.com\">Order now ...<\/a><\/strong><\/div><\/div><\/div><div class=\"clear-both\"><\/div><\/div><div class=\"wrap-top\"><div class=\"wrap-left\"><h4>Congenital myasthenic syndrome (CMS) - Russell Terrier<\/h4><p class=\"bodytext\">The <strong><em>CHRNE<\/em> gene<\/strong> encodes part of the acetylcholine receptor in the muscle cell membrane. If this receptor is defective, the <strong>muscle cells can no longer effectively receive and respond to nerve signals<\/strong>. Accordingly, affected puppies often develop marked <strong>signs of weakness<\/strong> under <strong>exertion<\/strong> at around <strong>4\u20135 weeks of age<\/strong>.<\/p><\/div><div class=\"wrap-right\"><div class=\"wrap-toggle\"><div class=\"toggle-details\"><details><summary class=\"summary-details\">Order details<\/summary><table border=\"0\"><tr><td width=\"45%\"><span><strong>Test number<\/strong><\/span><\/td><td>8206<\/td><\/tr><tr><td><strong>Sample material<\/strong><\/td><td>0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT)<\/td><\/tr><tr><td><strong>Test duration<\/strong><\/td><td>7-14 working days<\/td><\/tr><\/table><\/details><details><summary class=\"summary-specs\">Test specifications<\/summary><table border=\"0\"><tr><td width=\"45%\"><strong>Symptom complex<\/strong><\/td><td>muscular<\/td><\/tr><tr><td width=\"45%\"><strong>Inheritance<\/strong><\/td><td>autosomal recessive<\/td><\/tr><tr><td width=\"45%\"><strong>Age of onset<\/strong><\/td><td>5 weeks <\/td><\/tr><tr><td width=\"45%\"><strong>Causality<\/strong><\/td><td>causally<\/td><\/tr><tr><td width=\"45%\"><strong>Gene<\/strong><\/td><td>CHRNE<\/td><\/tr><tr><td width=\"45%\"><strong>Mutation<\/strong><\/td><td>INS<\/td><\/tr><tr><td width=\"45%\"><strong>Literature<\/strong><\/td><td><a href='https:\/\/www.omia.org\/OMIA000685\/9615\/' target='_blank'>OMIA:000685-9615<\/a><\/td><\/tr><\/table><\/details><\/div><div class=\"order-now\"><strong><a href=\"https:\/\/shop.labogen.com\">Order now ...<\/a><\/strong><\/div><\/div><\/div><div class=\"clear-both\"><\/div><\/div><div class=\"wrap-top\"><div class=\"wrap-left\"><h4>Congenital myasthenic syndrome (CMS) - Heideterrier<\/h4><p class=\"bodytext\"><p>In <strong>Heideterriers<\/strong>, the first signs often appear <strong>just a few days after birth<\/strong>. As early as <strong>a few days old<\/strong>, it may be noticeable that the puppies <strong>cannot properly coordinate their forelegs<\/strong> and that <strong>reflexes are diminished or absent<\/strong>.<\/p> <p>As the condition progresses, the affected animals develop a <strong>generalized muscle weakness<\/strong> that <strong>worsens throughout the day<\/strong>. Especially <strong>at night<\/strong>, the symptoms are usually <strong>most pronounced<\/strong>.<\/p> <p>In <strong>more severe cases<\/strong>, it may occur that the puppies <strong>fall over sideways<\/strong> or <strong>are not able to stand up<\/strong>. Despite these <strong>pronounced physical limitations<\/strong>, their <strong>awareness and playfulness remain intact<\/strong> \u2013 the animals appear alert and interested but <strong>cannot adequately control their muscles<\/strong>.<\/p><\/p><\/div><div class=\"wrap-right\"><div class=\"wrap-toggle\"><div class=\"toggle-details\"><details><summary class=\"summary-details\">Order details<\/summary><table border=\"0\"><tr><td width=\"45%\"><span><strong>Test number<\/strong><\/span><\/td><td>8206<\/td><\/tr><tr><td><strong>Sample material<\/strong><\/td><td>0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT)<\/td><\/tr><tr><td><strong>Test duration<\/strong><\/td><td>7-14 working days<\/td><\/tr><\/table><\/details><details><summary class=\"summary-specs\">Test specifications<\/summary><table border=\"0\"><tr><td width=\"45%\"><strong>Symptom complex<\/strong><\/td><td>muscular<\/td><\/tr><tr><td width=\"45%\"><strong>Inheritance<\/strong><\/td><td>autosomal recessive<\/td><\/tr><tr><td width=\"45%\"><strong>Age of onset<\/strong><\/td><td>2 weeks <\/td><\/tr><tr><td width=\"45%\"><strong>Causality<\/strong><\/td><td>causally<\/td><\/tr><tr><td width=\"45%\"><strong>Gene<\/strong><\/td><td>CHRNE<\/td><\/tr><tr><td width=\"45%\"><strong>Mutation<\/strong><\/td><td>DUP<\/td><\/tr><tr><td width=\"45%\"><strong>Literature<\/strong><\/td><td><a href='https:\/\/www.omia.org\/OMIA000685\/9615\/' target='_blank'>OMIA:000685-9615<\/a><\/td><\/tr><\/table><\/details><\/div><div class=\"order-now\"><strong><a href=\"https:\/\/shop.labogen.com\">Order now ...<\/a><\/strong><\/div><\/div><\/div><div class=\"clear-both\"><\/div><\/div><div style=\"margin-bottom: 50px; clear: both;\">&nbsp;<\/div>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":1,"featured_media":0,"parent":8791,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-248206","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/labogen.com\/en\/wp-json\/wp\/v2\/pages\/248206","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/labogen.com\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/labogen.com\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/labogen.com\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/labogen.com\/en\/wp-json\/wp\/v2\/comments?post=248206"}],"version-history":[{"count":0,"href":"https:\/\/labogen.com\/en\/wp-json\/wp\/v2\/pages\/248206\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/labogen.com\/en\/wp-json\/wp\/v2\/pages\/8791"}],"wp:attachment":[{"href":"https:\/\/labogen.com\/en\/wp-json\/wp\/v2\/media?parent=248206"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}