{"product_id":"ornithine-translocase-deficiency-test-in-hyderabad","title":"Ornithine Translocase Deficiency Test in Hyderabad","description":"\u003cp\u003e\u003cstrong\u003eIdentify\u003c\/strong\u003e genetic causes of urea cycle disorders with the \u003cstrong\u003eOrnithine Translocase Deficiency Test\u003c\/strong\u003e at Lucid Medical Diagnostics in Hyderabad. This advanced molecular genetic test detects mutations in the \u003cstrong\u003eSLC25A15 gene\u003c\/strong\u003e, which are associated with \u003cstrong\u003eornithine translocase deficiency (hyperornithinemia-hyperammonemia-homocitrullinuria syndrome)\u003c\/strong\u003e. The test helps diagnose inherited metabolic abnormalities affecting ammonia processing and protein metabolism, especially in individuals with unexplained hyperammonemia or related clinical symptoms. Using advanced molecular diagnostic technology and stringent quality standards, Lucid Medical Diagnostics delivers accurate, reliable, and timely results to assist clinicians in diagnosis, genetic counseling, and personalized management of metabolic disorders.\u003c\/p\u003e\n\u003cp\u003eHome Sample Collection Available\u003cbr\u003eGet Reports\u003cbr\u003e\u003c\/p\u003e","brand":"Lucid Medical Diagnostic Centre","offers":[{"title":"Default Title","offer_id":42057768927335,"sku":"LMD9350","price":18810.0,"currency_code":"INR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0635\/3970\/8007\/files\/WhatsAppImage2026-07-10at11.58.18_efe72fe8-196e-40ca-ae1d-76b05d1030c5.jpg?v=1783665801","url":"https:\/\/lucid-medical-diagnostic-centre.myshopify.com\/products\/ornithine-translocase-deficiency-test-in-hyderabad","provider":"Lucid Medical Diagnostic Centre","version":"1.0","type":"link"}