Oxford, United Kingdom – According to a study by Andrew Zisserman, a new program can now help the victims track rare genetic diseases just by looking at old family photographs.
Zisserman and his colleagues at the University of Oxford have devised a program that can run on 93 percent accuracy. This is still not enough for a diagnosis. However, it means so much more in minimizing the possibilities.
It can be a more time-efficient program. Urgent care clinics can know the procedures that they will have to conduct right there and then.
Marfan Syndrome for the Abraham Lincoln
Among the many examples stated by the researcher is the Marfan Syndrome found on Abraham Lincoln. This is among the rare genetic diseases that still have no cure until now. They were able to track down the disease just by looking at the photographs presented by the historians.
Only a few genetic diseases can be tracked down using tests. Even the best urgent care clinic in your town may not have the access to it. It is painful to just live by thee circumstances, especially that six percent of the world’s population is known to catch such illnesses. However, this all new program from Zisserman can make it a whole lot easier.
Tests can be time consuming and really expensive. This, however, can be very reliable even to countries that cannot access the expensive tests yet. This can be the cheapest yet most efficient urgent care that they can get.
A Breakthrough in the World of Medicine
Typically, there are scientists and experts who can read rare genetic diseases just by looking at photos as well. However, they are taking too long to process the entire examination. It could be weeks, months, even a year for some.
Families of those with such illnesses will never have a prolonged agony. They can focus more on the medication rather than the diagnosis. The urgent care near me provided by this system is not entirely brand new.
The software was derived from all the present systems that there is today. However, the program is something out of the books. It is so good that it can provide answers right after the child is born.
Rare genetic diseases have always been a problem. The lack of the information on where they are coming from has always caused a lot of medical distress. Will the medicine be the next to be invented?
