Fanconi Anemia - Get information and read articles on Fanconi Anemia signs, symptoms, causes, treatment, prevention and diagnosis at onlymyhealth.com, your complete health guide.
Fanconianemia is an inherited diseases that is spread from the parents to the child and it is therefore, one of the most common causes as well as risk factors for this disease.
Since fanconi anemia is an inherited disease and therefore, those people who have a family history of FA are the most likely to suffer from the disease among other factors.
Treatment options for fanconi anemia are decided based on how well or how poorly the patient's bone marrow is producing new cells and his/her age.
A diagnosis of FA is confirmed through genetic tests, including chromosome breakage testing, cytometric flow analysis, and mutation screening.
The overarching medical challenge that Fanconi patients face is a failure of their bone marrow to produce blood cells.
FA is an inherited disease. It's passed from parents to children through the genes. At least 13 faulty genes are associated with FA.
Fanconi anaemia is a rare, inherited blood disorder that leads to bone marrow failure. The condition is also referred to as Fanconi's anemia
The most common symptom of all types of anaemia is fatigue. The other symptoms include shortness of breath, dizziness, headache and chest pain.
An inherited blood disorder which can eventually lead to your bone marrow failure, understand how you can prevent it.