Marfan Syndrome Diagnosis: An Introduction
There is no specific laboratory test that is used to make a
Marfan syndrome diagnosis. Your doctor or geneticist (a doctor with special knowledge about inherited diseases) will rely on:
- Observation
- A complete medical history
- A physical exam
- Certain tests.
Marfan Syndrome Diagnosis: Medical History, Physical Exam, and Tests
In order to make a Marfan syndrome diagnosis, doctors begin by asking a number of questions (medical history). Your doctor will be looking for information regarding family members who may have Marfan syndrome or family members who had an early, unexplained heart-related death.
After the medical history, your doctor will perform a thorough physical examination, which will include an evaluation of the skeletal frame.
Your doctor may also do an eye examination, including a "slit lamp" evaluation and a heart test such as an echocardiogram (a test that uses ultrasound waves to examine the heart and aorta).
Marfan Syndrome Diagnosis: Criteria
Doctors can diagnose Marfan syndrome if the patient has a family history of the disease, and if there are specific problems in at least two of the body systems.
Patients who do not have a family history of Marfan syndrome must have problems in at least three body systems before a Marfan syndrome diagnosis will be made. In addition, two of the body systems must show clear signs that are relatively specific to Marfan syndrome.