Mediterranean fever is a serious genetic disease that causes frequent high temperature and pain in the abdomen and lungs, and is often diagnosed in childhood, according to the website. mayoclinic Tests and procedures used to diagnose familial Mediterranean fever include genetic testing and a review of the family medical history.
Mediterranean fever diagnostic tests
Physical exam: Your doctor may ask you about your signs and symptoms and do a physical exam to gather more information..
Review your family medical history: A family history of familial Mediterranean fever increases your likelihood of developing this condition because this genetic mutation is passed on from parents to their children..
Blood tests: During a seizure, blood tests may show elevated levels of certain signs that you have an inflammatory condition in your body. One of these signs is a high level of white blood cells that fight infections..
Genetic testing: Genetic testing may determine whether a gene is MEFV Yours has a mutation associated with familial Mediterranean fever.
Genetic tests are not advanced enough to test for every genetic mutation associated with FMF, so there is the potential for false negative results. For this reason, doctors do not usually use genetic testing as the only way to diagnose FMF..
There is no cure for familial Mediterranean fever. However, treatment can help prevent signs and symptoms.
Mediterranean fever symptoms
1: Severe rise in body temperature.
2: severe abdominal pain and inability to eat.
3:Chest pain and inability to breathe properly.
4:Severe swelling in muscles and joints.
5:The patient experiences rashes on the legs and knees.
6:Pain in muscles and joints.
7: Complications of the disease may arrive and cause kidney failure.
According to the website, Mediterranean fever occurs due to the presence of a genetic mutation that is transmitted from parents to children, and the mutation causes many problems, and there are also some factors that increase the risk of contracting the disease, most notably the presence of a family history of the disease.
