{"product_id":"egendhhg","title":"Hypogonadotropic Hypogonadism Panel","description":"The Hypogonadotropic Hypogonadism Panel analyzes genes that are associated with isolated gonadotropin-releasing hormone deficiency (IGD), Kallmann syndrome, and syndromes with hypogonadism as a presenting feature. These disorders result in low concentrations of gonadotropins (luteinizing and follicle-stimulating hormones) and hypogonadism. Some individuals with IGD have an impaired sense of smell; this combination of features is known as Kallmann syndrome. These genes were selected based on the available evidence to date to provide a broad analysis for inherited hypogonadotropic hypogonadism. The genetic heterogeneity associated with these conditions can make it difficult to use phenotype as the sole criterion to select a definitive cause. Broad panel testing allows for an efficient evaluation of several potential genes based on a single clinical indication. Genetic testing of these genes may confirm a diagnosis and help guide treatment and management decisions. \n\nIdentification of a disease-causing variant can inform recurrence-risk assessment and genetic counseling.","brand":"Medical Genetics Company","offers":[{"title":"Default Title","offer_id":44974152778014,"sku":"EGENDHHG","price":2550.0,"currency_code":"SAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/6678\/6590\/files\/enigma-test-icon-endocrinology-hormone-v1.png?v=1793571266","url":"https:\/\/shop.enigmagenomics.com\/en\/products\/egendhhg","provider":"Enigma Genomics","version":"1.0","type":"link"}