{"id":1445614,"date":"2020-10-16T11:36:27","date_gmt":"2020-10-16T09:36:27","guid":{"rendered":"https:\/\/staging-wp-int.laboklin.com\/products\/genetics\/hereditary-diseases\/horse\/lavender-foal-syndrome-lfs\/"},"modified":"2020-10-16T11:36:27","modified_gmt":"2020-10-16T09:36:27","slug":"lavender-foal-syndrome-lfs","status":"publish","type":"page","link":"https:\/\/laboklin.com\/fi\/products\/genetics\/hereditary-diseases\/horse\/lavender-foal-syndrome-lfs\/","title":{"rendered":"Lavender foal syndrome (LFS)"},"content":{"rendered":"

Lavender foal syndrome (LFS)<\/h3>

LABOKLIN Service ID: 8231<\/span><\/p>

LFS is an autosomal recessive inherited disease which has been reported mainly in the Egyptian Arabian.Affected foals can display an array of neurological signs including tetanic-like seizures, opisthotonus, stiff or paddling leg movements and nystagmus. These neurologic impairments prevent the foal from standing and nursing normally and, if not lethal on their own, are often the cause for euthanasia. In addition to these abnormalities, affected foals possess a characteristic diluted \u2018\u2018lavender\u2019\u2019 coat color. This resulting coat color, variously described as pale gray, pewter, and light chestnut, as well as lavender, has coined the name \u2018\u2018lavender foal syndrome\u2019\u2019 (LFS), also called \u2018\u2018coat color dilution lethal\u2019\u2019. There is currently no treatment for LFS available. Additionally, initial diagnosis can be difficult as the clinical signs of LFS can easily be confused with a number of neonatal conditions including neonatal maladjustment syndrome and encephalitis. <\/p>
Method<\/strong><\/td>

TaqMan SNP assay<\/p><\/td><\/tr>

Breed list<\/strong><\/td>

Arabian Horse<\/p><\/td><\/tr>

Heredity<\/strong><\/td>

autosomal recessive<\/p><\/td><\/tr>

Duration<\/strong><\/td>

3 - 5 days after arrival of the sample in the lab<\/p><\/td><\/tr><\/table>\n","protected":false},"excerpt":{"rendered":"

Lavender foal syndrome (LFS)LABOKLIN Service ID: 8231LFS is an autosomal recessive inherited disease which has been reported mainly in the Egyptian Arabian.Affected foals can display an array of neurological signs including tetanic-like seizures, opisthotonus, stiff or paddling leg movements and nystagmus. These neurologic impairments prevent the foal from standing and nursing normally and, if not…<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":1444941,"menu_order":19,"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-1445614","page","type-page","status-publish","hentry","description-off"],"_links":{"self":[{"href":"https:\/\/laboklin.com\/fi\/wp-json\/wp\/v2\/pages\/1445614","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/laboklin.com\/fi\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/laboklin.com\/fi\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/laboklin.com\/fi\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/laboklin.com\/fi\/wp-json\/wp\/v2\/comments?post=1445614"}],"version-history":[{"count":0,"href":"https:\/\/laboklin.com\/fi\/wp-json\/wp\/v2\/pages\/1445614\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/laboklin.com\/fi\/wp-json\/wp\/v2\/pages\/1444941"}],"wp:attachment":[{"href":"https:\/\/laboklin.com\/fi\/wp-json\/wp\/v2\/media?parent=1445614"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}