{"product_id":"egneunur","title":"Neuropathies Panel","description":"The Neuropathies Panel analyzes genes that are associated with hereditary neuropathies, including but not limited to Charcot-Marie-Tooth disease (CMT), hereditary motor neuropathy (HMN), and hereditary sensory and autonomic neuropathy (HSAN). The genetic heterogeneity associated with these conditions can make it difficult to use phenotype as the sole criterion to select a definitive cause. These genes were curated based on the available evidence to date in order to provide analysis for hereditary neuropathies. Given the clinical overlap of hereditary neuropathies, broad panel testing allows for an efficient evaluation of several potential genes based on a single clinical indication. \n\nSome genes in this test may also be associated with additional unrelated disorders which are not included in the list of disorders tested. Genetic testing of these genes may help confirm a clinical diagnosis, predict disease prognosis and progression, facilitate early detection of symptoms, inform family planning and genetic counseling, or promote enrollment in clinical trials.","brand":"Medical Genetics Company","offers":[{"title":"Default Title","offer_id":44974152024350,"sku":"EGNEUNUR","price":2550.0,"currency_code":"SAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/6678\/6590\/files\/enigma-test-icon-neurology-nerve-v1.png?v=1793571232","url":"https:\/\/shop.enigmagenomics.com\/en\/products\/egneunur","provider":"Enigma Genomics","version":"1.0","type":"link"}