{"product_id":"egmetnur","title":"Neurotransmitter Disorders Panel","description":"The Neurotransmitter Disorders Panel analyzes genes that are associated with disorders of neurotransmitter metabolism, receptors, and transporters including:\n\n- Disorders of monoamine synthesis, transport, or metabolism\n- BH4 synthesis\/recycling defects\n- Disorders of GABA synthesis, transport or metabolism, and GABA receptors\n- Defects in glutamate metabolism, receptor, or transporter that affect the central nervous system\n- Vitamin B6 \/ Pyridoxine disorders\n- Disorders of glycine metabolism with effect on the central nervous system, including glycine cleavage system\n- Serine biosynthesis disorders\n\nThis panel may be appropriate for patients with abnormal findings on CSF neurotransmitter studies and\/or neurological features that include a combination of dystonia, parkinsonism, autonomic and behavioral dysfunction, or oculogyric crises. \n\nThese genes were selected based on the available evidence to date to provide a broad test for neurotransmitter disorders. Genetic testing of these genes may confirm a diagnosis and help guide treatment and management decisions. Identification of a disease-causing variant could also guide testing and diagnosis of at-risk relatives.\n\n","brand":"Medical Genetics Company","offers":[{"title":"Default Title","offer_id":44974151303454,"sku":"EGMETNUR","price":2550.0,"currency_code":"SAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/6678\/6590\/files\/enigma-test-icon-metabolism-neuron-v1.png?v=1793571181","url":"https:\/\/shop.enigmagenomics.com\/en\/products\/egmetnur","provider":"Enigma Genomics","version":"1.0","type":"link"}