Your doctor or a genetic counselor they work with may give you the results. When the genetic testing analysis report is complete, it will be available to the ordering health care provider via the lab’s ordering portal. Test results are available to the ordering health care provider about four weeks after the DNA sample has been submitted. InformedDNA’s genetic counselors will send a summary of the consultation review to your physician after genetic counseling is complete. When InformedDNA receives the request for your results consultation conveyed by Blueprint’s test requisition process, they will notify you. InformedDNA, who are experts in the genetics of inherited retinal diseases, provides phone-based genetic counseling for the patient and family. If the doctor or clinic doesn’t provide genetic counseling (which is usually the case), they need to order no-cost genetic counseling services for you from InformedDNA. Genetic counseling is required by the sponsored program and will help you understand the results and what they mean for you and your family. You should ask your doctor who will provide your genetic counseling if you are not sure. That is, unless the doctor or their genetic counselor chooses to provide counseling. When the doctor orders the genetic test through the Blueprint website, they will likely need to order InformedDNA genetic counseling for you during the process. Make sure your doctor orders (or provides) genetic counseling. Patients and families should never contact Blueprint. If the doctor has questions, they should reach out directly to Blueprint. (Many doctors ordering the test for the first time order the wrong panel.) They need to order The My Retina Tracker Panel from the options on the ordering screen. Your doctor will order the test online from Blueprint Genetics using their Nucleus portal. Make sure your doctor orders the My Retina Tracker Panel ![]() For example, in some children or in anyone who has difficulty generating enough saliva to fill the saliva collection tube. However, there may be instances when a blood sample is required. Saliva, buccal (cheek), and blood sample kits will produce the same genetic testing results. Only saliva and buccal sample kits will be sent to homes. In this case, an office visit may not be necessary if you have had a recent exam with the doctor who is submitting your sample. The doctor can decide to have the DNA sample collection kit sent to your home. The doctor can order the kit ahead of time. ![]() Make sure the doctor has a sample collection kit before you arrive for your appointment. Though the genetic test is provided at no cost to the patient or the doctor, the patient is responsible for all other costs (for exams, tests, etc.) for the appointment. If you haven’t seen the doctor before, you will be considered a new patient and may need to undergo a complete exam. ![]() Your doctor will usually ask you to come in for an appointment (and eye exam) to collect the DNA sample (obtained via saliva or blood). Some doctors may not wish to participate in the program and they are not obligated to. You (the patient or family member) may need to help educate the doctor and/or the clinic staff about the program. Keep in mind: While some doctors may be familiar with the sponsored genetic testing program or are participating in it, others may not be familiar with the program or genetic testing. ![]() The program is only available to residents and doctors in the U.S. The doctors need to be able to clinically diagnose you (the patient) with an inherited retinal disease. can order the Foundation’s no-cost genetic test online from Blueprint Genetics ( Nucleus portal). Talk to your eye health care provider about genetic testing and whether the My Retina Tracker Genetic Testing Program is right for you.Īll MDs (ophthalmologists and retinal specialists) and most ODs (optometrists) in the U.S. This guide is for helping patients and families understand the ordering and testing process for the non-cost open access My Retina Tracker Genetic Testing Program. What is the My Retina Tracker ® Genetic Testing Program? A Guide for Patients The no-cost My Retina Tracker ® Genetic Testing Program is Sponsored by the Foundation Fighting Blindness and Blueprint GeneticsĪ genetic diagnosis can provide many benefits to people with inherited retinal diseases including: clarification of a clinical diagnosis, determination of the disease inheritance pattern within the family, and identification of clinical trials and therapies that may be appropriate for the patient. Vision and Eye Health Awareness Calendar.Virtual Workshop on Inflammation in Viral Gene Therapy of the Retina.Preclinical and Translational Research Webinar Series.Accessibility Statement, Tips & Guidelines.
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