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There is no cure for Marfan syndrome, but life expectancy has increased significantly over the last few decades [when?] and is now similar to that of the average person. [63] Regular checkups are recommended to monitor the health of the heart valves and the aorta. Marfan syndrome is treated by addressing each issue as it arises and, in ...
Marfan syndrome, cutis laxa syndrome, ... The median life expectancy in the population with vascular EDS is 48 years. [131] Complications. Vascular.
As with Marfan syndrome, people with CCA typically have an arm span that is greater than their height and very long fingers and toes. [2] However, Beals and Hecht discovered in 1972 that, unlike Marfan's, CCA is caused by mutations to the fibrillin-2 (FBN2) gene rather than the fibrillin-1 (FBN1) gene. [1] [3]
XYY syndrome, also known as Jacobs syndrome, is an aneuploid genetic condition in which a male has an extra Y chromosome. [1] There are usually few symptoms. [ 2 ] These may include being taller than average and an increased risk of learning disabilities .
Marfan syndrome may be considered due to the disproportion between limb and torso length observed in both syndromes, as well as both experiencing joint issues. Beckwith-Wiedemann syndrome, another disproportionate tall stature syndrome, can cause developmental disability similar to that seen in some cases of trisomy X. [38]
Keep in mind that friendships will ebb and flow throughout your life. Someone's going to get married, someone's going to move, everyone's going to grieve. "Navigating those shifts requires ...
A number of genetic conditions are associated with heart defects, including Down syndrome, Turner syndrome, and Marfan syndrome. [3] Congenital heart defects are divided into two main groups: cyanotic heart defects and non-cyanotic heart defects, depending on whether the child has the potential to turn bluish in color. [3]
The Oscars are set to be held at the Dolby Theatre in Los Angeles on March 2. (Matt Sayles/Invision/AP) (Matt Sayles/Invision/AP)