{"product_id":"sindrome-de-usher-panel-por-exoma-clinico-sec-cnvs-25-genes","title":"USHER SYNDROME: CLINICAL EXOME PANEL (Sec. \u0026amp; CNVs) – 25 genes","description":"\u003cp\u003eThe Usher Syndrome panel studies the genetic causes of the most common form of inherited deafblindness, characterized by congenital sensorineural hearing loss associated with retinitis pigmentosa and, in some cases, vestibular impairment. It includes genes involved in the function of the auditory sensory epithelium and retina, alterations in which lead to progressive dysfunction of photoreceptors and hair cells. Molecular analysis allows for the classification of the different clinical subtypes (Usher type I, II, and III), confirmation of the autosomal recessive inheritance pattern, and the provision of genetic counseling and visual prognosis. Genes analyzed include: MYO7A, USH2A, CDH23, PCDH15, ADGRV1, and others. You can consult the complete list of analyzed genes by contacting Genotica.\u003c\/p\u003e","brand":"LabGenetics","offers":[{"title":"Default Title","offer_id":52131444949258,"sku":null,"price":850.0,"currency_code":"EUR","in_stock":true}],"url":"https:\/\/www.genotica.com\/en\/products\/sindrome-de-usher-panel-por-exoma-clinico-sec-cnvs-25-genes","provider":"Genotica","version":"1.0","type":"link"}