What is Marfan Syndrome?
Marfan syndrome is a genetic condition primarily given away as a connective tissue disorder. The body’s internal organs are bound together by fibrous tissues that take no weight. Almost all of the body systems develop together with each other. The heart, eyes, skeletal system, and joints are among the main organs that bear the brunt of the disease. Marfan syndrome, the manifestation of a five-year-old girl in the study conducted by Dr. Antoine Marfan, was the first genetic disorder discovered in 1896.
