Doctor insights on:
Marijuana Marfan's Syndrome Treat
See below: Marfan syndrome is a disorder of connective tissue, the tissue that strengthens the body's structures. Disorders of connective tissue affect the skeletal system, cardiovascular system, eyes, and skin. Vision problems should be treated when possible. Monitor for scoliosis, especially during the teenage years. Medicine to slow the heart rate may help prevent stress on the aorta.
Marfans/ehler danlos: Marfan syndrome is a connective tissue disorder, tissues that strengthen bodies structures. In most cases it is inherited condition, but approx 30% of patients have no family history tall arms and height, affects lungs, heart and aorta, eyes causing cataract, skin problems, and tissue covering the spinal chord.
Genetic mutation: Marfan syndrome is caused by a gene mutation (in the fbn1 gene). A mutation leads to defective, weakened connective tissue throughout the body. Symptoms show up in the parts of the body where shape and structural integrity relies a lot on the weakened type of connective tissue.See 1 more doctor answer
Genetic disorder: Fbn1 gene controls connective tissue metabolism. If there are mutations or repeats, then marfa's will result. The symptoms are the result of malformed collagen. So dislocated lens in eye, heart valve problems, scoliosis, pneumothorax, artery problems may occur. Most cases are inherited, but occasionally marfan's occurs from a spontaneous mutation. This gene can be tested for in a blood specimen.See 1 more doctor answer
Having the features: Features suggestive of marfan syndrome include: above-average height, long arms, long fingers, flat feet, high-arched palate, narrow face, crowded teeth, small lower jaw, pectus carinatum (pigeon chest), pectus excavatum (sunken chest), hunchback (hunchback), scoliosis (crooked back), hypermobile/hyperflexible joints, etc... A person with several of these features can see a doctor for evaluation.See 1 more doctor answer
Www. Marfan. Org: Marfan syndrome is a genetic abnormality affecting the fbn1 gene. It is thought of as a "connective tissue" disease. People with marfan have varying levels of abnormalities of the skeleton, their heart, their eyes, and their lungs. The marfan foundation has a great website at www. Marfan. Org. At the site, there is important information about diagnosis, with recommendations.See 1 more doctor answer
Sometimes: Marfan syndrome is preventable when the adults who know they have marfan syndrome thoughtfully choose not to have biological children (50% of their children would have the disease). Some cases are not preventable, such as the 20-30% of marfan syndrome persons who have the disease from a new mutation (neither parent had a mutation).See 1 more doctor answer
Not usually: Marfan's snydrome affects the collagen in the body. In addition to risk of lens problems, the cornea (which is made mostly of collagen) can remain unstable throughout life. This can cause prescription changes after lasik, as well as other corneal problems. It is not recommended to have laser vision correction in patients with marfan's.See 4 more doctor answers
Marfan syndrome: There is no cure for this disorder. Treatment can slow progression & ameliorate symptoms, such as cardiovascular (aneurysms) or connective tissue changes (pain) etc.
Joint instability: Can lead to more joint pain in marian's patients but cramping is likely not associated.
Not that I know: The only likely association I can think is klinefelter's sydrome. But this is not close. Ks is only in males, they tend to be taller than average (similar to marfan's) and may have motor delays and learning problems (similar to autism). But they usually lack the main features of profound communication and social skills impairment of as. Many/most klindefelter's appear entirely normal.See 2 more doctor answers