I am 25 years old,
femaleCondoms
Female condoms
Female sexual dysfunction, been having chest pains off and on for years now. I have had two
nuclearNuclear ventriculography stress tests, many VQ scans, and a few years back even had some chest ct's. Recently, I also started having back pain with it. They are sending me for another VQ today at 3. And have mentioned the possibility of testing my aorta. A few questions ...
1. I had a stress test 2 weeks ago or so, should I be having a VQ scan so soon after that
radiationCystitis - noninfectious
Radiation therapy?
2. I'm trying to avoid anymore radition from ct so which imaging technique is better for imaging the aorta ... An MRI or an MRA? And should it be ordered with or without contrast? And is it just called a chest mri or mra or should it be called
cardiacCardiac catheterization
Cardiac tamponade
Left heart ventricular angiography mri or mra? I am asking because my doctor isn't
clearClear by design
Clear eyes
Clear eyes acr
Clear eyes clr
Clear-atadine
Clear-atadine children's about alternatives to ct.
3. That would just view the
thoracicEchocardiogram
Lung needle biopsy
Thoracic aortic aneurysm
Thoracic ct
Thoracic organs
Thoracic outlet anatomy
Thoracic outlet syndrome
Thoracic spine x-ray
Vertebra, thoracic (mid back) aorta, am I correct? What would be needed to view the abdominal as well? An ultrasound? And is that all that would be needed? A chest scan and stomach ultrasound? Then the entire aorta has been viewed?
4. If someone has a normal Echocardiogram except for trace regurge, what is the liklhood of Marfan's with no family history??? But I do have pectus, long fingers and toes, and very flexible joints.
Thanks so much.
My understanding is that an MRA is an MRI with contrast. Without contrast an MRI of the aorta does not show (or perhaps show as clearly) the delineation of the inner surface of the artery.
I was told by a genetic cardiologist who did assess me for Marfan Syndrome that with no family history of MFS, one major criteria met (aortic aneurysm w/root involvement), and a few minor minor indicators (tall, very nearsighted, wrist thumb sign, flexible), no pectus, no scoliosis, I had about a 12% chance of having MFS. Genetic testing (~$2K) showed I do not have a FBN1 mutation (which would indicate MFS). BTW about 1/4 of people diagnosed with MFS have a spontaneous mutation--meaning there is no family history or its occurence, as the doc said, is sporadic.
I